WO2022108670A1 - Multilayer films having at least one matte surface - Google Patents
Multilayer films having at least one matte surface Download PDFInfo
- Publication number
- WO2022108670A1 WO2022108670A1 PCT/US2021/053369 US2021053369W WO2022108670A1 WO 2022108670 A1 WO2022108670 A1 WO 2022108670A1 US 2021053369 W US2021053369 W US 2021053369W WO 2022108670 A1 WO2022108670 A1 WO 2022108670A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- polyethylene
- outer layer
- weight percent
- layer
- multilayer film
- Prior art date
Links
- -1 polyethylene Polymers 0.000 claims abstract description 121
- 229920000573 polyethylene Polymers 0.000 claims abstract description 101
- 239000004698 Polyethylene Substances 0.000 claims abstract description 97
- 229920001684 low density polyethylene Polymers 0.000 claims abstract description 78
- 229920000642 polymer Polymers 0.000 claims abstract description 75
- 239000004702 low-density polyethylene Substances 0.000 claims abstract description 73
- 239000002245 particle Substances 0.000 claims abstract description 63
- 239000000155 melt Substances 0.000 claims abstract description 38
- 239000000463 material Substances 0.000 claims abstract description 31
- 229920001903 high density polyethylene Polymers 0.000 claims description 23
- 239000004700 high-density polyethylene Substances 0.000 claims description 22
- 229920000098 polyolefin Polymers 0.000 claims description 19
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 7
- 150000008064 anhydrides Chemical group 0.000 claims description 4
- 229920001169 thermoplastic Polymers 0.000 claims description 4
- 239000004416 thermosoftening plastic Substances 0.000 claims description 4
- 229920000058 polyacrylate Polymers 0.000 claims description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 182
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- 239000000203 mixture Substances 0.000 description 33
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- 239000000126 substance Substances 0.000 description 18
- 239000003054 catalyst Substances 0.000 description 17
- 238000000034 method Methods 0.000 description 16
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 13
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- 239000000806 elastomer Substances 0.000 description 13
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- 239000013536 elastomeric material Substances 0.000 description 10
- 229920002647 polyamide Polymers 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 9
- 239000012792 core layer Substances 0.000 description 9
- 229920000092 linear low density polyethylene Polymers 0.000 description 9
- 229920000034 Plastomer Polymers 0.000 description 8
- 150000001993 dienes Chemical class 0.000 description 8
- 239000004707 linear low-density polyethylene Substances 0.000 description 7
- 239000000565 sealant Substances 0.000 description 7
- 229920002554 vinyl polymer Polymers 0.000 description 7
- 230000004888 barrier function Effects 0.000 description 6
- 235000013305 food Nutrition 0.000 description 6
- 229920001179 medium density polyethylene Polymers 0.000 description 6
- 239000004701 medium-density polyethylene Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- HOYUQSOBHNSRER-UHFFFAOYSA-N ethenyl cyanate Chemical compound C=COC#N HOYUQSOBHNSRER-UHFFFAOYSA-N 0.000 description 5
- 230000009477 glass transition Effects 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 229920001296 polysiloxane Polymers 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 229920005601 base polymer Polymers 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 239000012968 metallocene catalyst Substances 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000012986 chain transfer agent Substances 0.000 description 3
- 239000011258 core-shell material Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
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- 229920002959 polymer blend Polymers 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 239000004287 Dehydroacetic acid Substances 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 2
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 2
- 150000003926 acrylamides Chemical class 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 150000008360 acrylonitriles Chemical class 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 150000008378 aryl ethers Chemical class 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000002981 blocking agent Substances 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000007771 core particle Substances 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000002667 nucleating agent Substances 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 150000003016 phosphoric acids Chemical group 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
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- 239000010420 shell particle Substances 0.000 description 2
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- 239000012748 slip agent Substances 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 150000003440 styrenes Chemical class 0.000 description 2
- 229940124543 ultraviolet light absorber Drugs 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical compound CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- CTTJWXVQRJUJQW-UHFFFAOYSA-N 2,2-dioctyl-3-sulfobutanedioic acid Chemical compound CCCCCCCCC(C(O)=O)(C(C(O)=O)S(O)(=O)=O)CCCCCCCC CTTJWXVQRJUJQW-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- JJRUAPNVLBABCN-UHFFFAOYSA-N 2-(ethenoxymethyl)oxirane Chemical compound C=COCC1CO1 JJRUAPNVLBABCN-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ZXABMDQSAABDMG-UHFFFAOYSA-N 3-ethenoxyprop-1-ene Chemical compound C=CCOC=C ZXABMDQSAABDMG-UHFFFAOYSA-N 0.000 description 1
- PTHLSIBOMNYSIS-UHFFFAOYSA-N 5-(4-aminophenyl)-8-chloro-3-methyl-1,2,4,5-tetrahydro-3-benzazepin-7-ol Chemical compound C1N(C)CCC2=CC(Cl)=C(O)C=C2C1C1=CC=C(N)C=C1 PTHLSIBOMNYSIS-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
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- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical group OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229920003314 Elvaloy® Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- 240000002129 Malva sylvestris Species 0.000 description 1
- 235000006770 Malva sylvestris Nutrition 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229920010346 Very Low Density Polyethylene (VLDPE) Polymers 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 238000000333 X-ray scattering Methods 0.000 description 1
- 239000011954 Ziegler–Natta catalyst Substances 0.000 description 1
- YMOONIIMQBGTDU-VOTSOKGWSA-N [(e)-2-bromoethenyl]benzene Chemical compound Br\C=C\C1=CC=CC=C1 YMOONIIMQBGTDU-VOTSOKGWSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000007973 cyanuric acids Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000001739 density measurement Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- VVYDVQWJZWRVPE-UHFFFAOYSA-L dimethyltin(2+);diiodide Chemical compound C[Sn](C)(I)I VVYDVQWJZWRVPE-UHFFFAOYSA-L 0.000 description 1
- 229960000878 docusate sodium Drugs 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 238000001941 electron spectroscopy Methods 0.000 description 1
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- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical group CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Chemical group CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical group CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005638 polyethylene monopolymer Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004886 process control Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
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- 239000008117 stearic acid Chemical group 0.000 description 1
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
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Definitions
- This disclosure relates to multilayer films having at least one matte surface and to articles, such as labels and packages, comprising multilayer films having at least one matte surface.
- matte surface Polymer films having a matte surface are commonly used in a variety of applications.
- Optical properties, such as matte surface may be defined in terms of surface gloss and haze.
- a matte surface may be characterized by lower gloss and higher haze values as discussed further herein.
- Packaging applications such as pouches and bags for pet food, snack food, and the like, sometime utilize polymer films having a matte surface.
- the matte surface can be obtained through blends of incompatible polyolefins, generally by using blends of polyethylene and polypropylene.
- these incompatible blends of polyethylene and polypropylene create issues with process control. Specifically, when using different machine procedures for blending the incompatible polyolefins, the properties of the film product may be unpredictable and inconsistent.
- the present invention provides multilayer films that have a matte surface and that, in some embodiments, have desirable mechanical properties.
- multilayer films of the present invention have particularly low surface gloss values in an outer layer to provide a matte surface.
- multilayer films of the present invention have particularly low gloss values in an outer surface while maintaining desirable mechanical properties.
- multilayer films of the present invention having a matte surface can provide other advantages in some embodiments, such as reduced blocking and/or potential improved adhesion in lamination.
- the present invention provides a multilayer film having at least one matte surface that comprises (a) an outer layer comprising (i) 30 to 99.5 weight percent of a first low density polyethylene having a density of 0.919 g/cm 3 to 0.940 g/cm 3 and a melt index (I2) of 0.3 to 5 g/10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a first polyethylene having a density of 0.925 g/cm 3 to 0.970 g/cm 3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the outer layer; and (b) a second layer in adhering contact with the outer layer comprising (i) 1
- the present invention also provides articles, such as labels and packages, formed from any of the inventive multilayer films disclosed herein.
- composition refers to a mixture of materials which comprises the composition, as well as reaction products and decomposition products formed from the materials of the composition.
- Polymer means a polymeric compound prepared by polymerizing monomers, whether of the same or a different type.
- the generic term polymer thus embraces the term homopolymer (employed to refer to polymers prepared from only one type of monomer, with the understanding that trace amounts of impurities can be incorporated into the polymer structure), and the term interpolymer as defined hereinafter. Trace amounts of impurities (for example, catalyst residues) may be incorporated into and/or within the polymer.
- a polymer may be a single polymer, a polymer blend or a polymer mixture, including mixtures of polymers that are formed in situ during polymerization.
- interpolymer refers to polymers prepared by the polymerization of at least two different types of monomers.
- the generic term interpolymer thus includes copolymers (employed to refer to polymers prepared from two different types of monomers), and polymers prepared from more than two different types of monomers.
- olefin-based polymer or “polyolefin”, as used herein, refer to a polymer that comprises, in polymerized form, a majority amount of olefin monomer, for example ethylene or propylene (based on the weight of the polymer), and optionally may comprise one or more comonomers.
- ethylene/a-olefin interpolymer refers to an interpolymer that comprises, in polymerized form, a majority amount (>50 mol %) of units derived from ethylene monomer, and the remaining units derived from one or more a-olefins.
- Typical a- olefins used in forming ethylene/a-olefin interpolymers are C3-C10 alkenes.
- ethylene/a-olefin copolymer refers to a copolymer that comprises, in polymerized form, a majority amount (>50 mol %) of ethylene monomer, and an a-olefin, as the only two monomer types.
- a-olefin refers to an alkene having a double bond at the primary or alpha (a) position.
- Polyethylene or “ethylene-based polymer” shall mean polymers comprising a majority amount (>50 mol %) of units which have been derived from ethylene monomer. This includes polyethylene homopolymers, ethylene/a-olefin interpolymers, and ethylene/a- olefin copolymers. Common forms of polyethylene known in the art include Low Density Polyethylene (LDPE); Linear Low Density Polyethylene (LLDPE); Ultra Low Density Polyethylene (ULDPE); Very Low Density Polyethylene (VLDPE); Medium Density Polyethylene (MDPE); High Density Polyethylene (HDPE); Enhanced Polyethylene; polyethylene elastomers; and polyethylene plastomers. These polyethylene materials are generally known in the art; however, the following descriptions may be helpful in understanding the differences between some of these different polyethylene resins.
- LDPE Low Density Polyethylene
- LLDPE Linear Low Density Polyethylene
- ULDPE Ultra Low Density Polyethylene
- VLDPE Very Low Den
- LDPE may also be referred to as “high pressure ethylene polymer” or “highly branched polyethylene” and is defined to mean that the polymer is partly or entirely homo-polymerized or copolymerized in autoclave or tubular reactors at pressures above 14,500 psi (100 MPa) with the use of free-radical initiators, such as peroxides (see for example US 4,599,392, which is hereby incorporated by reference).
- LDPE resins typically have a density in the range of 0.916 to 0.935 g/cm 3 .
- LLDPE includes both resin made using the traditional Ziegler-Natta catalyst systems and chromium-based catalyst systems as well as single-site catalysts, including, but not limited to, bis -metallocene catalysts (sometimes referred to as “m- LLDPE”), constrained geometry catalysts (CGC), and molecular catalysts.
- Resins include linear, substantially linear, or heterogeneous polyethylene copolymers or homopolymers. LLDPEs contain less long chain branching than LDPEs and includes the substantially linear ethylene polymers which are further defined in U.S. Patent 5,272,236, U.S. Patent 5,278,272, U.S.
- Patent 5,582,923 and US Patent 5,733,155 the homogeneously branched linear ethylene polymer compositions such as those in U.S. Patent No. 3,645,992; the heterogeneously branched ethylene polymers such as those prepared according to the process disclosed in U.S. Patent No. 4,076,698; and/or blends thereof (such as those disclosed in US 3,914,342 or US 5,854,045).
- the LLDPEs can be made via gas-phase, solution-phase or slurry polymerization or any combination thereof, using any type of reactor or reactor configuration known in the art.
- MDPE refers to polyethylenes having densities from 0.926 to 0.940 g/cm 3 .
- MDPE is typically made using chromium or Ziegler-Natta catalysts or using singlesite catalysts including, but not limited to, bis-metallocene catalysts, constrained geometry catalysts, and molecular catalysts, and typically have a molecular weight distribution (“MWD”) greater than 2.5.
- MWD molecular weight distribution
- HDPE refers to polyethylenes having densities greater than about 0.940 g/cm 3 and up to about 0.970 g/cm 3 , which are generally prepared with Ziegler-Natta catalysts, chrome catalysts or single-site catalysts including, but not limited to, bis-metallocene catalysts and constrained geometry catalysts.
- ULDPE refers to polyethylenes having densities of 0.880 to 0.912 g/cm 3 , which are generally prepared with Ziegler-Natta catalysts, chrome catalysts, or single-site catalysts including, but not limited to, bis -metallocene catalysts and constrained geometry catalysts.
- Polyethylene plastomers/elastomers are substantially linear, or linear, ethylene/a- olefin copolymers containing homogeneous short-chain branching distributions comprising units derived from ethylene and units derived from at least one C3-C10 a-olefin comonomer, or at least one C4-C8 a-olefin comonomer, or at least one Ce-Cs a-olefin comonomer.
- Polyethylene plastomers/elastomers have a density from 0.870 g/cm 3 , or 0.880 g/ cm 3 , or 0.890 g/ cm 3 to 0.900 g/ cm 3 , or 0.902 g/ cm 3 , or 0.904 g/ cm 3 , or 0.909 g/ cm 3 , or 0.910 g/ cm 3 , or 0.917 g/ cm 3 .
- Nonlimiting examples of polyethylene plastomers/ elastomers include AFFINITYTM plastomers and elastomers (available from The Dow Chemical Company), EXACT Plastomers (available from ExxonMobil Chemical), Tafmer (available from Mitsui), NexleneTM (available from SK Chemicals Co.), and Lucene (available LG Chem Ltd.).
- Blends mean a composition of two or more polymers. Such a blend may or may not be miscible. Such a blend may or may not be phase separated. Such a blend may or may not contain one or more domain configurations, as determined from transmission electron spectroscopy, light scattering, x-ray scattering, and any other method known in the art. Blends are not laminates, but one or more layers of a laminate may contain a blend. Such blends can be prepared as dry blends, formed in situ (e.g., in a reactor), melt blends, or using other techniques known to those of skill in the art.
- adhering contact and like terms mean that one facial surface of one layer and one facial surface of another layer are in touching and binding contact to one another such that one layer cannot be removed from the other layer without damage to the interlayer surfaces (i.e., the in-contact facial surfaces) of both layers.
- compositions claimed through use of the term “comprising” may include any additional additive, adjuvant, or compound, whether polymeric or otherwise, unless stated to the contrary.
- the term, “consisting essentially of’ excludes from the scope of any succeeding recitation any other component, step or procedure, excepting those that are not essential to operability.
- the term “consisting of’ excludes any component, step or procedure not specifically delineated or listed.
- the present invention relates to multilayer films having at least one matte surface and to labels and packages formed from such multilayer films.
- the matte surface can provide a desirable appearance and in some embodiments, the multilayer films can also have desirable mechanical properties.
- the present invention provides a multilayer film having at least one matte surface that comprises (a) an outer layer comprising (i) 30 to 99.5 weight percent of a first low density polyethylene having a density of 0.919 g/cm 3 to 0.940 g/cm 3 and a melt index (I2) of 0.3 to 5 g/10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a first polyethylene having a density of 0.925 g/cm 3 to 0.970 g/cm 3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the outer layer; and (b) a second layer in adhering contact with the outer layer comprising (i) 1
- outer layer comprises 80 to 90 weight percent of the first low density polyethylene, based on the weight of the outer layer.
- the first low density polyethylene in the outer layer has a density of 0.930 to 0.940 g/cm 3 and/or a melt index (I2) of 2.5 to 4 g/10 minutes.
- the first polyethylene is present in the outer layer in an amount up to 50 weight percent.
- the first polyethylene is present in the outer layer in an amount up to 20 weight percent.
- the first polyethylene in the outer layer has a density of 0.60 to 0.970 g/cm 3 and a melt index (I2) of 6 to 10 g/10 minutes.
- the first polymeric material of the core of the polymer particle is elastomeric and the second polymeric material of the shell of the polymer particle is a thermoplastic.
- the shell in some embodiments, comprises an acrylic polymer.
- the polymer particles have an average size of 1 to 10 microns.
- the outer layer further comprises a compatibilizer.
- the compatibilizer when present, in some embodiments, is a polyolefin copolymer with acrylic acid, a polyolefin copolymer with an acrylate, a polyolefin copolymer with a maleic anhydride ester, or a polyolefin copolymer grafted with one or more anhydride group, acrylate group or carboxylic acid group.
- the compatibilizer is maleic anhydride grafted low density polyethylene or a maleic anhydride grafted high density polyethylene.
- the compatibilizer is present in the outer layer in an amount up to 10 weight percent based on the total weight of the outer layer.
- the first polyethylene (in the outer layer) and the second polyethylene (in the second layer) are each high density polyethylene.
- the multilayer film has two matte surfaces, wherein the multilayer film has a second outer layer, wherein the second layer is between the outer layer and the second outer layer, and wherein the second outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°.
- the second outer layer comprises (i) 30 to 99.5 weight percent of a low density polyethylene having a density of 0.919 g/cm 3 to 0.940 g/cm 3 and a melt index (I2) of 0.3 to 5 g/10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a polyethylene having a density of 0.925 g/cm 3 to 0.970 g/cm 3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the second outer layer.
- the present invention also provides articles, such as labels and packages, formed from any of the inventive multilayer films disclosed herein.
- the outer layer in a multilayer film advantageously provides a matte surface.
- the term “matte surface” refers to a surface with a dull appearance, as opposed to a glossy appearance.
- a matte surface has one or both of (1) a gloss of less than 50%, and (2) a haze of greater than 45%.
- the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°.
- the outer layer has a gloss of less than 45% as measured by ASTM D2457 at an angle of 45°.
- the outer layer has a haze of greater than 45% as measured by ASTM D1003.
- the outer layer has a haze of greater than 50% as measured by ASTM D1003.
- the outer layer has a haze of greater than 55% as measured by ASTM DI 003.
- the outer layer comprises (i) 30 to 99.5 weight percent of a first low density polyethylene having a density of 0.919 g/cm 3 to 0.940 g/cm 3 and a melt index (I2) of 0.3 to 5 g/10 minutes, and (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, each based on the total weight of the outer layer.
- the outer layer further comprises up to 50 weight percent of a first polyethylene having a density of 0.925 g/cm 3 to 0.970 g/cm 3 and a melt index (I2) of 0.8 to 10 g/10 minutes, based on the total weight of the outer layer.
- the outer layer further comprises a compatibilizer.
- the outer layer includes a first low density polyethylene having a density of 0.919 to 0.940 g/cm 3 . All individual values and subranges of 0.919 to 0.940 g/cm 3 are included herein and disclosed herein; for example, the density of the low density polyethylene can be from a lower limit of 0.919, 0.920, 0.922, 0.925, 0.927, 0.929, or 0.930 g/ cm 3 to an upper limit of 0.925, 0.930, 0.935, or 0.940 g/cm 3 . In some embodiments, the low density polyethylene has a density of 0.930 to 0.940 g/cm 3 .
- the low density polyethylene has a melt index (I2) 0.3 to 5 g/10 minutes. All individual values and subranges from 0.3 to 5 g/10 minutes are included herein and disclosed herein.
- the low density polyethylene can have an I2 from a lower limit of 0.3, 0.5, 0.7, 0.9, 1.0, 1.2, 1.5, 1.8, 2.0, 2.3, 2.5, 2.7, 3.0, 3.3, or 3.5 g/10 minutes to an upper limit of 2.0, 2.5, 2.8, 3.0, 3.2, 3.5, 3.7, 4.0, 4.2, 4.5, 4.8, or 5 g/10 minutes.
- the low density polyethylene can have an I2 of 2.5 to 4.0 g/10 minutes.
- the outer layer comprises from 30 to 99.5 wt% of the low density polyethylene, based on the total weight of the outer layer. All individual values and subranges from 30 to 99.5 percent by weight (wt%) are included herein and disclosed herein; for example the amount of the low density polyethylene can be from a lower limit of 30, 35, 40, 45, 50, 55, 60, 65, 70, 76, 80, 85, or 90 wt% to an upper limit of 50, 55, 60, 65, 70, 75, 80, 85, 90, 92, 94, 96, 98, 99, or 99.5 wt%. For example, the amount of the low density polyethylene can be from 50 to 95 wt%, or in the alternative, from 70 to 95 wt%, or in the alternative, from 70 to 90 wt%, or in the alternative from 80 to 90 wt%.
- low density polyethylenes examples include DOWTM low density polyethylenes (LDPE) commercially available from The Dow Chemical Company, such as DOWTM LDPE 525E, DOWTM LDPE 410E, DOWTM LDPE 421E, DOWTM LDPE 545E, DOWTM LDPE 555E, and DOWTM LDPE 515E.
- LDPE low density polyethylenes
- the outer layer also comprises 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index.
- the core/shell polymeric particles are present in amounts of at least 0.1, at least 0.5, or at least 1 weight percent based on total weight of the outer layer.
- the core/shell polymeric particles are present in amounts of no more than 20, no more than 15, no more than 10, no more than 7, or no more than 5 weight percent based on total weight of the outer layer.
- the particles can have an average particle size of at least 0.5 or at least 1 micron and no more than 15, no more than 12, or no more than 10 microns.
- Particle size can be determined by using conventional methods, e.g. use of a particle sizer such as Model BL90 from Brookhaven Instrument. Particle size can be measured in powder state. Particle size can show the size of agglomerated core shell particles.
- Core-shell particles may be purchased with a nominal particle size as specified by the vendor.
- the core/shell particles can be formed from acrylic monomers such as butyl acrylate, 2-ethylhexyl acrylate and lauryl methacrylate.
- the core/shell polymeric particles can be characterized in that polymer in the core has a different refractive index from the refractive index of the polymer in the shell.
- the refractive index of the polymer in the core can differ from the refractive index of the polymer in the shell by at least 0.02 or at least 0.03.
- Refractive index can be measured using a refractometer and following ASTM D542.
- the core shell material can be pressed into a thin film by hot press to facilitate this measurement.
- the core/shell particles can have an elastomeric core with a thermoplastic shell.
- the particle can have a rubber particle core formed by a polymer comprising an elastomeric or rubbery polymer as a main ingredient, optionally an intermediate layer formed with a monomer having two or more double bonds and coated on the core layer, and a shell layer formed by a polymer graft polymerized on the core or on an intermediate layer.
- the shell layer partially or entirely covers the surface of the rubber particle core by graft polymerizing a monomer to the core.
- At least 30%, at least 40%, at least 50% or at least 60% up to 95, up to 90 up to 85 or up to 80% of the weight of the particle can be the core.
- the polymer constituting the rubber particle core can have a glass transition temperature (T g ) of 0° C or lower or -30° C or lower.
- wi and W2 refer to the weight fraction of the two comonomers
- T g ⁇ i) and T g (2) refer to the glass transition temperatures of the two corresponding homopolymers in Kelvin.
- T g of a polymer phase can also be calculated by using the appropriate values for the glass transition temperatures of homopolymers, which may be found, for example, in “Polymer Handbook”, edited by J. Brandrup and E. H. Immergut, Interscience Publishers.
- the polymer constituting the rubber particle core can be made from an elastomeric material comprising from 50 weight percent to 100 weight percent of at least one member selected from diene monomers (conjugated diene monomers) and (meth)acrylic acid ester monomers and 0 to 50 weight percent of other copolymerizable vinyl monomers, polysiloxane type elastomers or combinations thereof wherein the weight percents are based on total weight of the elastomeric material.
- diene monomers conjuggated diene monomers
- (meth)acrylic acid ester monomers and 0 to 50 weight percent of other copolymerizable vinyl monomers, polysiloxane type elastomers or combinations thereof wherein the weight percents are based on total weight of the elastomeric material.
- (meth)acryl is defined as acryl and/or methacryl.
- the diene monomer (conjugated diene monomer) used in making the elastomeric material can include but is not limited to, for example, butadiene, isoprene and chloroprene. Butadiene can be used in some embodiments.
- the (meth)acrylic ester monomer can include, for example, butyl acrylate, 2-ethylhexyl acrylate, and lauryl methacrylate, and can be used alone or in combination.
- the above-mentioned elastomeric materials of a diene monomer or (meth) acrylate ester monomer can also be a copolymer of a vinyl monomer copolymerizable therewith.
- the vinyl monomer copolymerizable with the diene monomer or (meth)acrylic ester monomers can include, for example, aromatic vinyl monomers and vinyl cyanate monomers. Examples of aromatic vinyl monomers that can be used include but are not limited to styrene, alpha-methylstyrene, and vinyl naphthalene, while examples of vinyl cyanate monomers that can be used include but are not limited to (meth) acrylonitrile and substituted acrylonitrile. The aromatic vinyl monomers and vinyl cyanate monomers can be used alone or in combination.
- the amount of the diene monomer or (meth)acrylic ester monomer used can be in the range of from 50 weight percent to 100 weight percent or from 60 weight percent to 100 weight percent based on the entire weight of the elastomeric material. If the amount of the diene monomer or (meth)acrylic ester monomer to be used for the entire rubber elastomer is less than 50 weight percent, the ability of the polymer particles to toughen a polymer network, such as a cured epoxy matrix, is decreased.
- the amount of the monomer copolymerizable therewith can be 50 weight percent or less or 40 weight percent or less based on the entire weight of the elastomeric material.
- a polyfunctional monomer can also be included for controlling the degree of crosslinking.
- the polyfunctional monomer can include, for example, divinylbenzene, butanediol di(meth)acrylate, triallyl (iso)cyanurate, allyl(meth) acrylic, diallyl itaconate, and diallyl phthalate.
- the polyfunctional monomer can be used in an amount in the range of from 0 weight percent to 10 weight percent, from 0 weight percent to 3 weight percent, or from 0 weight percent to 0.3 weight percent, based on the entire weight of the elastomeric material. In the case where the amount of the polyfunctional monomer exceeds 10 weight percent, the ability of the polymer particles to toughen a polymer network can be decreased.
- a chain transfer agent can be used for controlling the molecular weight or the crosslinking density of the polymer constituting the elastomeric material.
- the chain transfer agent can include, for example, an alkylmercaptan containing from 5 to 20 carbon atoms.
- the amount of the chain transfer agent in the recipe can be in the range of from 0 weight percent to 5 weight percent, or from 0 weight percent to 3 weight percent based on the entire weight of the elastomeric material. In the case where the amount exceeds 5 weight percent, the amount of the non-crosslinked portion in the rubber particle core increases, which can result in undesired effects on the heat resistance, rigidity, etc. of the composition when it is incorporated into an epoxy resin composition.
- a polysiloxane type elastomer can be used in place of the elastomeric material described above as the rubber particle core or in combination therewith.
- a polysiloxane type elastomer constituted of dialkyl or diaryl substituted silyloxy unit, for example, dimethyl silyloxy, methylphenyl silyloxy, and diphenyl silyloxy can be used.
- a crosslinked structure can be introduced by using a polyfunctional alkoxy silane compound or with radial polymerization of silane compound having a vinylic reactive group.
- the polymer particles can be configured to have an intermediate layer between an elastic core layer and a shell layer.
- the intermediate layer is formed by using a monomer (hereinafter, sometimes referred to as a “monomer for intermediate layer formation”) having two or more polymerizable (radical polymerizable) double bonds in a single molecule.
- a monomer for intermediate layer formation having two or more polymerizable (radical polymerizable) double bonds in a single molecule.
- the monomer for intermediate layer formation is graft- polymerized with a polymer forming the elastic core layer to substantially chemically bond the intermediate layer and the shell layer and, at the same time, through the remaining double bond(s), can crosslink the surface of the elastic core layer or can bond to the shell layer. This can improve the grafting efficiency of the shell layer, since many double bonds are arranged in the elastic core layer.
- the intermediate layer is present in an amount of from 0 or from 0.2 weight percent to 7 weight percent of the polymer particles.
- the monomer having two or more double bonds and can be selected from the group consisting of (meth) acrylate type polyfunctional monomers, isocyanuric acid derivatives, aromatic vinyl type polyfunctional monomers, and aromatic polycarboxylic acid esters. Radical polymerizable double bonds are more efficient to form a crosslinked layer that covers surface of the elastic core layer.
- the mass of the monomers forming the intermediate layer equals the mass of the intermediate layer, assuming all monomers added to the formulation participated in the reaction to form the intermediate layer.
- the shell layer can be graft polymerized with the polymer constituting the rubber particle core, substantially forming a chemical bond with the polymer constituting the core directly or via the intermediate layer. At least 70 weight percent, at least 80 weight percent, or at least 90 weight percent of the polymer constituting the shell layer can be bonded with the core.
- the polymer constituting the shell layer can be a polymer or copolymer obtained by polymerizing or copolymerizing one or more ingredients selected from the group consisting of (meth)acrylic esters, aromatic vinyl compounds, vinyl cyanate compounds, unsaturated acid derivatives, (meth)acrylamide derivatives and maleimide derivatives.
- (meth)acrylic esters that can be used include, but are not limited to alky l(meth) acrylate esters such as methyl(meth)acrylate, ethyl(meth)acrylate, butyl(meth)acrylate, and 2-ethylhexyl(meth)acrylate.
- aromatic vinyl compounds include, but are not limited to styrene, a-methylstyrene, alkyl-substituted styrene, and halogen-substituted styrenes such as bromo styrene or chloro styrene.
- Examples of vinyl cyanate compounds include, but are not limited to (meth) acrylonitrile and substituted acrylonitrile.
- Examples of the monomers containing the reactive functional group include, but are not limited to 2-hydroxylethyl (meth)acrylate, 2- aminoethyl(meth)acrylate, glycidyl(meth)acrylate, and (meth) acrylate esters having a reactive side chain.
- Examples of the vinyl ether containing a reactive group include but are not limited to glycidyl vinyl ether and allyl vinyl ether.
- Examples of the unsaturated carboxylic acid derivatives include but are not limited to (meth)acrylic acid, itaconic acid, chrotonic acid and maleic acid anhydride.
- Examples of (meth)acrylamide derivatives include, but are not limited to (meth)acrylamide (including N-substituted products).
- maleimide derivatives include but are not limited to maleic acid imide (including N-substitution products).
- the shell polymer can comprise at least 5, at least 10, at least 15 or at least 20% up to 70, up to 60, or up to 50% by weight based on total weight of the particle.
- the weight ratio of the core layer to the shell layer of a preferred rubber particle can be in the range of from at least 30:70, at least 40:60, or at least 50:50 up to 95:5, up to 90:10, up to 85:15, or up to 80:20.
- the shell can have a T g of at least 50, at least 70, or at least 100 °C.
- the core/shell polymer particles can be produced by a variety of well-known methods, for example, emulsion polymerization, suspension polymerization, or microsuspension polymerization. Among them, a production process by the emulsion polymerization is suitable from the view point that it is easy to design composition of the core/shell polymer particles, and it is easy to produce the particles at an industrial scale and maintain quality of the rubbery polymer particles suitable to the process of this invention.
- the emulsifying or dispersing agent in an aqueous medium it is preferred to use those that maintain emulsifying or dispersion stability even in the case where pH of the aqueous latex is neutral.
- nonionic emulsifier or dispersant such as alkali metal salts or ammonium salts of various acids
- alkyl or aryl sulfonic acids typically represented by dioctyl sulfosuccinic acid or dodecylbenzene sulfonic acid
- alkyl or aryl sulfonic acid typically represented by dodecyl sulfonic acid
- alkyl or aryl ether sulfonic acid alkyl or aryl substituted phosphoric acid
- alkyl or aryl ether substituted phosphoric acid alkyl or aryl ether substituted phosphoric acid
- N-alkyl or aryl sarcosinic acid typically represented by dodecyl sarcosinic acid
- alkyl or aryl carboxylic acid typically represented by oleic acid or stearic acid
- alkyl or aryl ether carboxylic acids alkyl or aryl substitute
- the particle can have an alkylacrylate copolymer core surrounded by a methyl methacrylate copolymer shell.
- the particle can have a core with a T g of less than 0 °C and the shell has a T g of at least 100 °C.
- Commercially available particles that are suitable include PARALOIDTM EXL 5136 from The Dow Chemical Company.
- the outer layer can comprise more than one (e.g., 2 or 3) types of polymeric particle as described above.
- the outer layer may further comprise a first polyethylene having a density of 0.925 g/cm 3 to 0.970 g/cm 3 and a melt index (D) of 0.8 to 10 g/10 minutes.
- the first polyethylene is different from the first low density polyethylene having a density of 0.919 g/cm 3 to 0.940 g/cm 3 and a melt index (I2) of 0.3 to 5 g/10 minutes discussed above.
- the first polyethylene that may be used in the outer layer has a density of 0.925 to 0.970 g/cm 3 . All individual values and subranges of 0.925 to 0.970 g/cm 3 are included herein and disclosed herein; for example, the density of the first polyethylene can be from a lower limit of 0.925, 0.930, 0.935, 0.940, 0.945, 0.950, 0.955, or 0.960 g/ cm 3 to an upper limit of 0.945, 0.950, 0.955, 0.960, 0.965, or 0.970 g/cm 3 . In some embodiments, the first polyethylene has a density of 0.960 to 0.970 g/cm 3 .
- the first polyethylene has a melt index (I2) 0.8 to 10 g/10 minutes. All individual values and subranges from 0.8 to 10 g/10 minutes are included herein and disclosed herein.
- the first polyethylene can have an I2 from a lower limit of 0.8, 1.0, 1.2, 1.5, 1.8, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, or 6.5 g/10 minutes to an upper limit of 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, or 10 g/10 minutes.
- the first polyethylene can have an I2 of 6 to 10 g/10 minutes.
- the first polyethylene can be an optional component in the outer in some embodiments.
- the outer layer comprises up to 50 wt% of the first polyethylene, based on the total weight of the outer layer. All individual values and subranges up to 50 percent by weight (wt%) are included herein and disclosed herein; for example the amount of the first polyethylene can be from a lower limit of 1, 3, 5, 10, 15, 20, 25, 30, 35 or 40 wt% to an upper limit of 5, 10, 15, 20, 25, 30, 35, 40, 45, or 50.
- the amount of the first polyethylene can be up to 20 wt%, or in the alternative, from 1 to 20 wt%, or in the alternative, from 5 to 20 wt%.
- polyethylenes that can be used as the first polyethylene in the outer layer include, for example, low density polyethylene, linear low density polyethylene, medium density polyethylene, enhanced polyethylene, and high density polyethylene.
- the first polyethylene is a high density polyethylene.
- commercially available polyethylenes that can be used as the first polyethylene include DOWLEXTM 2006G high density polyethylene, ELITETM 5960G1 enhanced polyethylene, DOWLEXTM 2750ST high density polyethylene, ELITETM 5940ST enhanced polyethylene, DOWLEXTM 2740G polyethylene, DOWLEXTM 2062GC polyethylene, and ELITETM AT 6900 enhanced polyethylene, each of which are available from The Dow Chemical Company.
- the outer layer of the inventive multilayer film further comprises a compatibilizer.
- the compatibilizer can advantageously provide a smooth dispersion of the polymer particles within the base resin (e.g., the first low density polyethylene and any additional polyethylene).
- the compatibilizer is a polymer characterized in that it has similar chemical structure to the base polymer and has pendant and/or end groups that have an affinity to the core/shell polymer particle.
- the compatibilizer can be the same class of polyolefin (e.g. if the base polymer is a polyethylene the compatibilizer advantageously can be a polyethylene functionalized with a group having affinity to the shell material).
- the compatibilizer can be a polyolefin/acrylate copolymer (e.g., polyethylene/acrylate copolymer such as ELVALOY ACTM from The Dow Chemical Company) or a polyolefin/acrylic acid copolymer (e.g., polyethylene/acrylic acid copolymer such as NUCRELTM from The Dow Chemical Company), or a polyolefin/carboxylic acid copolymer, or a polyolefin/maleic anhydride ester copolymer.
- a polyolefin based compatibilizer can be grafted with one or more anhydride groups or acrylate groups or acrylic acid groups.
- the compatibilizer can be a polyethylene such as an LDPE or HDPE grafted with an anhydride group such as maleic anhydride.
- anhydride group such as maleic anhydride.
- FUSABONDTM E265 from The Dow Chemical Company.
- the amount of compatibilizer can be from 0.5 or from 1 weight percent up to 30, up to 20, up to 15, or up to 10 weight percent based on total weight of the outer layer. In some embodiments, the amount of compatibilizer is 0.5 to 10 weight percent based on the total weight of the outer layer.
- the amount of the compatibilizer may increase as the amount of acrylic polymer particle increases.
- the compatibilizer can be a mixture of polymers as described above as compatibilizers.
- the outer layer of the multilayer film may contain one or more additives as is generally known in the art.
- additives include antioxidants, such as IRGANOX 1010 and IRGAFOS 168 (commercially available from BASF), ultraviolet light absorbers, antistatic agents, pigments, dyes, nucleating agents, fillers, slip agents, fire retardants, plasticizers, processing aids, lubricants, stabilizers, smoke inhibitors, viscosity control agents, surface modification agents, and anti-blocking agents.
- Multilayer films according to embodiments of the present invention further comprise a second layer in adhering contact with the outer surface.
- the second layer comprises (i) 1 to 80 weight percent of a second low density polyethylene having a density of 0.919 g/cm 3 to 0.940 g/cm 3 and a melt index (I2) of 0.3 to 5 g/10 minutes, and (ii) 20 to 99 weight percent of a second polyethylene having a density of 0.925 g/cm 3 to 0.970 g/cm 3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the outer layer.
- the second low density polyethylene used in the second layer is the same as the first low density polyethylene used in the outer layer (i.e., the same density, melt index (I2), and polymeric architecture). In some embodiments, the second polyethylene used in the second layer is the same as the first polyethylene used in the outer layer (i.e., the same density, melt index (I2), and polymeric architecture). In some embodiments, the second low density polyethylene used in the second layer is the same as the first low density polyethylene used in the outer layer, and the second polyethylene used in the second layer is the same as the first polyethylene used in the outer layer.
- the low density polyethylene having a density of 0.919 to 0.940 g/cm 3 .
- All individual values and subranges of 0.919 to 0.940 g/cm 3 are included herein and disclosed herein; for example, the density of the second low density polyethylene can be from a lower limit of 0.919, 0.920, 0.922, 0.925, 0.927, 0.929, or 0.930 g/ cm 3 to an upper limit of 0.925, 0.930, 0.935, or 0.940 g/cm 3 .
- the second low density polyethylene has a density of 0.930 to 0.940 g/cm 3 .
- the second low density polyethylene has a melt index (I2) 0.3 to 5 g/10 minutes. All individual values and subranges from 0.3 to 5 g/10 minutes are included herein and disclosed herein.
- the second low density polyethylene can have an I2 from a lower limit of 0.3, 0.5, 0.7, 0.9, 1.0, 1.2, 1.5, 1.8, 2.0, 2.3, 2.5, 2.7, 3.0, 3.3, or 3.5 g/10 minutes to an upper limit of 2.0, 2.5, 2.8, 3.0, 3.2, 3.5, 3.7, 4.0, 4.2, 4.5, 4.8, or 5 g/10 minutes.
- the second low density polyethylene can have an I2 of 2.5 to 4.0 g/10 minutes.
- the second layer comprises from 1 to 100 wt% of the second low density polyethylene, based on the total weight of the second layer. All individual values and subranges from 1 to 80 percent by weight (wt%) are included herein and disclosed herein; for example the amount of the second low density polyethylene can be from a lower limit of 1, 3, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, or 60 wt% to an upper limit of 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, or 80 wt%.
- the amount of the second low density polyethylene can be from 50 to 100 wt%, or in the alternative, from 60 to 100 wt%, or in the alternative, from 70 to 100 wt%.
- low density polyethylenes examples include DOWTM low density polyethylenes (LDPE) commercially available from The Dow Chemical Company, such as DOWTM LDPE 525E, DOWTM LDPE 410E, DOWTM LDPE 421E, DOWTM LDPE 545E, DOWTM LDPE 555E, and DOWTM LDPE 515E.
- LDPE low density polyethylenes
- the second layer also comprises a second polyethylene having a density of 0.925 g/cm 3 to 0.970 g/cm 3 and a melt index (I2) of 0.8 to 10 g/10 minutes.
- the second polyethylene is different from the second low density polyethylene having a density of 0.919 g/cm 3 to 0.940 g/cm 3 and a melt index (I2) of 0.3 to 5 g/10 minutes discussed above.
- the second polyethylene in the second layer can be the same as the first polyethylene used in the outer layer.
- both the first polyethylene used in the outer layer and the second polyethylene used in the second layer can be high density polyethylenes.
- the second polyethylene that may be used in the outer layer has a density of 0.925 to 0.970 g/cm 3 . All individual values and subranges of 0.925 to 0.970 g/cm 3 are included herein and disclosed herein; for example, the density of the second polyethylene can be from a lower limit of 0.925, 0.930, 0.935, 0.940, 0.945, 0.950, 0.955, or 0.960 g/ cm 3 to an upper limit of 0.945, 0.950, 0.955, 0.960, 0.965, or 0.970 g/cm 3 . In some embodiments, the second polyethylene has a density of 0.960 to 0.970 g/cm 3 .
- the second polyethylene has a melt index (I2) 0.8 to 10 g/10 minutes. All individual values and subranges from 0.8 to 10 g/10 minutes are included herein and disclosed herein.
- the second polyethylene can have an I2 from a lower limit of 0.8, 1.0, 1.2, 1.5, 1.8, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, or 6.5 g/10 minutes to an upper limit of 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, or 10 g/10 minutes.
- the second polyethylene can have an I2 of 6 to 10 g/10 minutes.
- the second layer comprises from 20 to 99 wt% of the second polyethylene, based on the total weight of the second layer. All individual values and subranges from 20 to 99 percent by weight (wt%) are included herein and disclosed herein; for example the amount of the second polyethylene can be from a lower limit of 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 76, or 80 wt% to an upper limit of 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 99 wt%.
- the amount of the second polyethylene can be from 1 to 50 wt%, or in the alternative, from 1 to 40 wt%, or in the alternative, from 1 to 30 wt%.
- polyethylenes that can be used as the second polyethylene in the second layer include, for example, low density polyethylene, linear low density polyethylene, medium density polyethylene, enhanced polyethylene, and high density polyethylene.
- the second polyethylene is a high density polyethylene.
- commercially available polyethylenes that can be used as the second polyethylene include DOWLEXTM 2006G high density polyethylene, ELITETM 5960G1 enhanced polyethylene, DOWLEXTM 2750ST high density polyethylene, ELITETM 5940ST enhanced polyethylene, DOWLEXTM 2740G polyethylene, DOWLEXTM 2062GC polyethylene, and ELITETM AT 6900 enhanced polyethylene, each of which are available from The Dow Chemical Company.
- the second layer of the multilayer film may contain one or more additives as is generally known in the art.
- additives include antioxidants, such as IRGANOX 1010 and IRGAFOS 168 (commercially available from BASF), ultraviolet light absorbers, antistatic agents, pigments, dyes, nucleating agents, fillers, slip agents, fire retardants, plasticizers, processing aids, lubricants, stabilizers, smoke inhibitors, viscosity control agents, surface modification agents, and anti-blocking agents.
- Multilayer films of the present invention can comprise a variety of other layers in addition to the outer layer and the second layer. Such layers would be in adhering contact with the second layer or another intervening layer.
- the number of layers in the multilayer film can depend on a number of factors including, for example, the desired properties of the film, the end use application, the desired thickness of the film, and others.
- the other layers when the multilayer film is to be used in package may be different from the other layers used when the multilayer film is to be used as a label. Examples of different layers that can be used in various embodiments are discussed further herein.
- Multilayer films of the present invention comprise up to 13 layers in some embodiments. In various embodiments, the multilayer film comprises 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13 layers.
- a multilayer film of the present invention comprises a second outer layer which is a sealant layer.
- the sealant layer can be used to form an article or package by using the sealant layer to adhere the film to another film, to a laminate, or to itself.
- the sealant layer can comprise any resins known to those having ordinary skill in the art to be useful as a sealant layer.
- polymers that can be used to form a sealant layer in some embodiments of the present invention include, without limitation, LDPE (e.g., DOWTM LDPE and AGILITYTM LDPE commercially available from The Dow Chemical Company), LLDPE (e.g., DOWLEXTM LLDPE resins commercially available from The Dow Chemical Company), polyolefin plastomers or elastomers (e.g., AFFINITYTM plastomers and elastomers commercially available from The Dow Chemical Company), ethylene vinyl acetate copolymers (e.g., ELVAXTM ethylene vinyl acetate copolymers commercially available from The Dow Chemical Company) and ionomers of ethylene acid copolymers (e.g., SURLYNTM ionomers commercially available from The Dow Chemical Company).
- LDPE e.g., DOWTM LDPE and AGILITYTM LDPE commercially available from The Dow Chemical Company
- LLDPE e.g.,
- the multilayer film comprises a second outer layer that provides a second matte surface.
- the second outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°.
- the composition of the second outer layer is the same as the composition of the first outer layer.
- the second outer layer comprises (i) 30 to 99.5 weight percent of a low density polyethylene having a density of 0.919 g/cm 3 to 0.940 g/cm 3 and a melt index (I2) of 0.3 to 5 g/ 10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a polyethylene having a density of 0.925 g/cm 3 to 0.970 g/cm 3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the second outer layer.
- the multilayer film is a five layer structure wherein a first outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45° to provide the matte surface.
- a core or innermost layer has the composition of the second layer as described above.
- a second outer layer in some embodiments, can provide a second matte surface (a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°) or can be a sealant layer as described above.
- Two intermediate or sub-skin layers are present with one intermediate layer between the first outer layer and the core layer, and a second intermediate layer between the second outer layer and the core layer.
- the intermediate layers can be formed from high density polyethylene or a blend of high density polyethylene and linear low density polyethylene (with HDPE being present in the larger amount).
- the film can comprise other layers such as barrier layers.
- barrier layers can comprise, for example, polyamide, ethylene vinyl alcohol copolymer, and other polymers used in barrier layers as known to those of skill in the art.
- an inner layer of the multilayer film comprises ethylene vinyl alcohol copolymer or polyamide.
- the multilayer film comprises 30 weight percent or less ethylene vinyl alcohol copolymer and polyamide based on the total weight of the multilayer film.
- the multilayer film comprises 20 weight percent or less ethylene vinyl alcohol copolymer and polyamide based on the total weight of the multilayer film. In some embodiments, the multilayer film comprises 10 weight percent or less ethylene vinyl alcohol copolymer and polyamide based on the total weight of the multilayer film. In some embodiments, the multilayer film comprises less than 5% by weight ethylene vinyl alcohol copolymer and polyamide based on the total weight of the multilayer film.
- one or more tie layers may be included in the film to adhere the barrier layer(s) to the polyethylene-based layer(s) as known to those of skill in the art based on the teachings herein.
- tie layer compositions can be used to form a tie layer as known to those of skill in the art based on the teachings herein.
- barrier properties may not be as important for the multilayer film.
- the multilayer film may comprise less than 0.5 weight percent ethylene vinyl alcohol copolymer and polyamide based on the total weight of the film. In some embodiments, the multilayer film comprises less than 0.1 weight percent ethylene vinyl alcohol copolymer and polyamide based on the total weight of the film. In some embodiments, the multilayer film is free of ethylene vinyl alcohol copolymer and polyamide.
- a multilayer film of the present invention has a total thickness of at least 30 microns. In some embodiments, the multilayer film has a thickness of up to 90 microns. In some embodiments, the multilayer film has a thickness from 30 microns to 90 microns.
- Multilayer films of the present invention can exhibit one or more desirable properties.
- the multilayer films of the present invention has a matte surface.
- the outer layer of the multilayer film provides a matte surface in that the outer layer has one or both of (1) a gloss of less than 50%, and (2) a haze of greater than 45%.
- the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°.
- the outer layer has a gloss of less than 45% as measured by ASTM D2457 at an angle of 45°.
- the outer layer has a haze of greater than 45% as measured by ASTM DI 003.
- the outer layer has a haze of greater than 50% as measured by ASTM D1003. In some embodiments, the outer layer has a haze of greater than 55% as measured by ASTM D1003. In some embodiments, the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45° and haze of greater than 45% as measured by ASTM DI 003. In some embodiments, the outer layer has a gloss of less than 45% as measured by ASTM D2457 at an angle of 45° and haze of greater than 50% as measured by ASTM D1003. In some embodiments, the outer layer has a gloss of less than 45% as measured by ASTM D2457 at an angle of 45° and haze of greater than 55% as measured by ASTM D1003.
- Multilayer films can be coextruded as blown films or cast films using techniques known to those of skill in the art based on the teachings herein.
- blown film manufacturing lines and cast film manufacturing lines can be configured to coextrude multilayer films of the present invention in a single extrusion step using techniques known to those of skill in the art based on the teachings herein.
- Embodiments of the present invention also comprise labels formed from or incorporating multilayer films of the present invention.
- Such labels can be made from the inventive multilayer films using techniques known to those having ordinary skill in the art based on the teachings herein.
- Embodiments of the present invention also comprise packages formed from or incorporating multilayer films of the present invention. Such packages can be made from the inventive multilayer films using techniques known to those having ordinary skill in the art based on the teachings herein.
- packages can include flexible packages, pouches, stand-up pouches, and pre-made packages or pouches.
- multilayer films of the present invention can be used for food packages.
- food that can be included in such packages include meats, cheeses, cereal, nuts, juices, sauces, and others.
- Such packages can be formed using techniques known to those of skill in the art based on the teachings herein and based on the particular use for the package (e.g., type of food, amount of food, etc.).
- Samples for density measurement were prepared according to ASTM D4703. Measurements were made, according to ASTM D792, Method B, within one hour of sample pressing.
- Haze was measured according to ASTM D 1003. A Hazegard Plus (BYK-Gardner USA; Columbia, MD) was used for testing. For each test, 5 samples were examined, and an average was reported. An area having a diameter of six centimeters was measured on each film sample.
- Elmendorf tear strength in the machine and cross directions are measured in accordance with ASTM D1922.
- the force in grams required to propagate tearing across a film or sheeting specimen is measured using a precisely calibrated pendulum device. Acting by gravity, the pendulum swings through an arc, tearing the specimen from a precut slit. The specimen is held on one side by the pendulum and on the other side by a stationary member. The loss in energy by the pendulum is indicated by a pointer or by an electronic scale. The scale indication is a function of the force required to tear the specimen.
- the sample used is the ‘constant radius geometry’ as specified in D1922. Testing would be typically carried out on samples that have been cut from both the MD and CD directions.
- DOWTM LDPE 525E low density polyethylene having a density of 0.9315 g/cm 3 and a melt index (I2) of 3.2 g/10 minutes.
- Polymer Particles polymer particles having a core and a shell structure.
- the polymeric material used in the core is elastomeric and has a glass transition temperature (T g ) of ⁇ 0 °C.
- the polymeric material used in the shell is thermoplastic and has a glass transition temperature (T g ) of > 100 °C.
- the polymeric material in the core has a refractive index that is different from the refractive index of the polymeric material in the shell.
- the average particle size of the Polymer Particles is between 1 and 10 microns.
- FUSABONDTM E265 High density polyethylene grafted with maleic anhydride having a density of 0.950 g/cm 3 and a melt index (I2) of 12 g/10 minutes. Each of these materials are commercially available from The Dow Chemical Company.
- the Polymer Particles are melt blended with the LDPE and Compatibilizer (if present) prior to being provided to the blown film line.
- the blends are melt blended on a Buss Kneader Compounder at 120 rpm (kneader speed), 3 amps (motor current), 5 kg/h, 60 rpm (screw speed), and a temperature profile of 110 °C/130 °C/140 °C/120 °C/125 °C.
- the above Comparative and Inventive Films are coextruded on a Dr. Collin 3 -layer Coextrusion Blown Film line.
- the nominal film thickness is 80 microns.
- the line was comprised of three 25:1 L/D single screw extruders, equipped with grooved feed zones.
- Screw diameters are 25 mm for the two outer layer extruders and 30 mm for the inner layer extruder (formed from Layer B).
- the melt temperature is 180° C-21O 0 C.
- the die diameter is 30 mm, and the die gap is 1.8 mm.
- the blow-up ratio is 2.5:1.
- the output rate is 15 kg/hour.
- the gloss at 45° and the haze of the Comparative and Inventive Films are measured as described in the Test Methods section. The results are shown in Table 2:
Abstract
Embodiments of the present invention relate to multilayer films, labels, and packages. In one aspect, a multilayer film having at least one matte surface comprises (a) an outer layer comprising (i) 30 to 99.5 weight percent of a first low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a first polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the outer layer; and (b) a second layer in adhering contact with the outer layer comprising (i) 1 to 80 weight percent of a second low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, and (ii) 20 to 99 weight percent of a second polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the second layer; wherein the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°.
Description
MULTILAYER FILMS HAVING AT LEAST ONE MATTE SURFACE
Field
This disclosure relates to multilayer films having at least one matte surface and to articles, such as labels and packages, comprising multilayer films having at least one matte surface.
Introduction
Polymer films having a matte surface are commonly used in a variety of applications. Optical properties, such as matte surface, may be defined in terms of surface gloss and haze. A matte surface may be characterized by lower gloss and higher haze values as discussed further herein.
Packaging applications, such as pouches and bags for pet food, snack food, and the like, sometime utilize polymer films having a matte surface. The matte surface can be obtained through blends of incompatible polyolefins, generally by using blends of polyethylene and polypropylene. However, these incompatible blends of polyethylene and polypropylene create issues with process control. Specifically, when using different machine procedures for blending the incompatible polyolefins, the properties of the film product may be unpredictable and inconsistent.
There is also interest in polyethylene films having a matte surface for use in labels. The development of labels has been traditionally focused on improving the homogeneity of the material together with the product or surface. Traditionally, mostly glossy labels were considered professional and of high quality. However, the marketplace is changing and naturally appearing, non-shiny textures are increasingly important. For example, labels having a non-glossy finish have been used to transport a message of high quality, organic products in some instances. A common approach to provide natural looking surfaces and natural appearance is to provide rough surfaces. This can be done by using inorganic fillers, but can also worsen the mechanical properties of the label.
There remains a need for new multilayer films having a matte surface and acceptable mechanical properties that can be used in labels and/or packaging applications.
Summary
The present invention provides multilayer films that have a matte surface and that, in some embodiments, have desirable mechanical properties. In some embodiments, multilayer films of the present invention have particularly low surface gloss values in an outer layer to
provide a matte surface. In some embodiments, multilayer films of the present invention have particularly low gloss values in an outer surface while maintaining desirable mechanical properties. In addition to providing a desirable appearance for some applications, multilayer films of the present invention having a matte surface can provide other advantages in some embodiments, such as reduced blocking and/or potential improved adhesion in lamination.
In one aspect, the present invention provides a multilayer film having at least one matte surface that comprises (a) an outer layer comprising (i) 30 to 99.5 weight percent of a first low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a first polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the outer layer; and (b) a second layer in adhering contact with the outer layer comprising (i) 1 to 80 weight percent of a second low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, and (ii) 20 to 99 weight percent of a second polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the second layer; wherein the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°.
As discussed below, the present invention also provides articles, such as labels and packages, formed from any of the inventive multilayer films disclosed herein.
These and other embodiments are described in more detail in the Detailed Description.
Detailed Description
Unless stated to the contrary, implicit from the context, or customary in the art, all parts and percents are based on weight, all temperatures are in 0 C, and all test methods are current as of the filing date of this disclosure.
The term “composition,” as used herein, refers to a mixture of materials which comprises the composition, as well as reaction products and decomposition products formed from the materials of the composition.
“Polymer” means a polymeric compound prepared by polymerizing monomers, whether of the same or a different type. The generic term polymer thus embraces the term homopolymer (employed to refer to polymers prepared from only one type of monomer, with the understanding that trace amounts of impurities can be incorporated into the polymer structure), and the term interpolymer as defined hereinafter. Trace amounts of impurities (for example, catalyst residues) may be incorporated into and/or within the polymer. A polymer may be a single polymer, a polymer blend or a polymer mixture, including mixtures of polymers that are formed in situ during polymerization.
The term “interpolymer,” as used herein, refers to polymers prepared by the polymerization of at least two different types of monomers. The generic term interpolymer thus includes copolymers (employed to refer to polymers prepared from two different types of monomers), and polymers prepared from more than two different types of monomers.
The terms “olefin-based polymer” or “polyolefin”, as used herein, refer to a polymer that comprises, in polymerized form, a majority amount of olefin monomer, for example ethylene or propylene (based on the weight of the polymer), and optionally may comprise one or more comonomers.
The term, “ethylene/a-olefin interpolymer,” as used herein, refers to an interpolymer that comprises, in polymerized form, a majority amount (>50 mol %) of units derived from ethylene monomer, and the remaining units derived from one or more a-olefins. Typical a- olefins used in forming ethylene/a-olefin interpolymers are C3-C10 alkenes.
The term, “ethylene/a-olefin copolymer,” as used herein, refers to a copolymer that comprises, in polymerized form, a majority amount (>50 mol %) of ethylene monomer, and an a-olefin, as the only two monomer types.
The term “a-olefin”, as used herein, refers to an alkene having a double bond at the primary or alpha (a) position.
“Polyethylene” or “ethylene-based polymer” shall mean polymers comprising a majority amount (>50 mol %) of units which have been derived from ethylene monomer. This includes polyethylene homopolymers, ethylene/a-olefin interpolymers, and ethylene/a- olefin copolymers. Common forms of polyethylene known in the art include Low Density Polyethylene (LDPE); Linear Low Density Polyethylene (LLDPE); Ultra Low Density Polyethylene (ULDPE); Very Low Density Polyethylene (VLDPE); Medium Density Polyethylene (MDPE); High Density Polyethylene (HDPE); Enhanced Polyethylene;
polyethylene elastomers; and polyethylene plastomers. These polyethylene materials are generally known in the art; however, the following descriptions may be helpful in understanding the differences between some of these different polyethylene resins.
The term “LDPE” may also be referred to as “high pressure ethylene polymer” or “highly branched polyethylene” and is defined to mean that the polymer is partly or entirely homo-polymerized or copolymerized in autoclave or tubular reactors at pressures above 14,500 psi (100 MPa) with the use of free-radical initiators, such as peroxides (see for example US 4,599,392, which is hereby incorporated by reference). LDPE resins typically have a density in the range of 0.916 to 0.935 g/cm3.
The term “LLDPE”, includes both resin made using the traditional Ziegler-Natta catalyst systems and chromium-based catalyst systems as well as single-site catalysts, including, but not limited to, bis -metallocene catalysts (sometimes referred to as “m- LLDPE”), constrained geometry catalysts (CGC), and molecular catalysts. Resins include linear, substantially linear, or heterogeneous polyethylene copolymers or homopolymers. LLDPEs contain less long chain branching than LDPEs and includes the substantially linear ethylene polymers which are further defined in U.S. Patent 5,272,236, U.S. Patent 5,278,272, U.S. Patent 5,582,923 and US Patent 5,733,155; the homogeneously branched linear ethylene polymer compositions such as those in U.S. Patent No. 3,645,992; the heterogeneously branched ethylene polymers such as those prepared according to the process disclosed in U.S. Patent No. 4,076,698; and/or blends thereof (such as those disclosed in US 3,914,342 or US 5,854,045). The LLDPEs can be made via gas-phase, solution-phase or slurry polymerization or any combination thereof, using any type of reactor or reactor configuration known in the art.
The term “MDPE” refers to polyethylenes having densities from 0.926 to 0.940 g/cm3. “MDPE” is typically made using chromium or Ziegler-Natta catalysts or using singlesite catalysts including, but not limited to, bis-metallocene catalysts, constrained geometry catalysts, and molecular catalysts, and typically have a molecular weight distribution (“MWD”) greater than 2.5.
The term “HDPE” refers to polyethylenes having densities greater than about 0.940 g/cm3 and up to about 0.970 g/cm3, which are generally prepared with Ziegler-Natta catalysts, chrome catalysts or single-site catalysts including, but not limited to, bis-metallocene catalysts and constrained geometry catalysts.
The term “ULDPE” refers to polyethylenes having densities of 0.880 to 0.912 g/cm3, which are generally prepared with Ziegler-Natta catalysts, chrome catalysts, or single-site catalysts including, but not limited to, bis -metallocene catalysts and constrained geometry catalysts.
"Polyethylene plastomers/elastomers" are substantially linear, or linear, ethylene/a- olefin copolymers containing homogeneous short-chain branching distributions comprising units derived from ethylene and units derived from at least one C3-C10 a-olefin comonomer, or at least one C4-C8 a-olefin comonomer, or at least one Ce-Cs a-olefin comonomer. Polyethylene plastomers/elastomers have a density from 0.870 g/cm3, or 0.880 g/ cm3, or 0.890 g/ cm3 to 0.900 g/ cm3, or 0.902 g/ cm3, or 0.904 g/ cm3, or 0.909 g/ cm3, or 0.910 g/ cm3, or 0.917 g/ cm3. Nonlimiting examples of polyethylene plastomers/ elastomers include AFFINITY™ plastomers and elastomers (available from The Dow Chemical Company), EXACT Plastomers (available from ExxonMobil Chemical), Tafmer (available from Mitsui), Nexlene™ (available from SK Chemicals Co.), and Lucene (available LG Chem Ltd.).
“Blend”, “polymer blend” and like terms mean a composition of two or more polymers. Such a blend may or may not be miscible. Such a blend may or may not be phase separated. Such a blend may or may not contain one or more domain configurations, as determined from transmission electron spectroscopy, light scattering, x-ray scattering, and any other method known in the art. Blends are not laminates, but one or more layers of a laminate may contain a blend. Such blends can be prepared as dry blends, formed in situ (e.g., in a reactor), melt blends, or using other techniques known to those of skill in the art.
The term “in adhering contact” and like terms mean that one facial surface of one layer and one facial surface of another layer are in touching and binding contact to one another such that one layer cannot be removed from the other layer without damage to the interlayer surfaces (i.e., the in-contact facial surfaces) of both layers.
The terms “comprising,” “including,” “having,” and their derivatives, are not intended to exclude the presence of any additional component, step or procedure, whether or not the same is specifically disclosed. In order to avoid any doubt, all compositions claimed through use of the term “comprising” may include any additional additive, adjuvant, or compound, whether polymeric or otherwise, unless stated to the contrary. In contrast, the term, “consisting essentially of’ excludes from the scope of any succeeding recitation any other component, step or procedure, excepting those that are not essential to operability. The term
“consisting of’ excludes any component, step or procedure not specifically delineated or listed.
The present invention relates to multilayer films having at least one matte surface and to labels and packages formed from such multilayer films. The matte surface can provide a desirable appearance and in some embodiments, the multilayer films can also have desirable mechanical properties.
In one embodiment, the present invention provides a multilayer film having at least one matte surface that comprises (a) an outer layer comprising (i) 30 to 99.5 weight percent of a first low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a first polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the outer layer; and (b) a second layer in adhering contact with the outer layer comprising (i) 1 to 80 weight percent of a second low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, and (ii) 20 to 99 weight percent of a second polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the second layer; wherein the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°. In some embodiments, outer layer comprises 80 to 90 weight percent of the first low density polyethylene, based on the weight of the outer layer. In some embodiments, the first low density polyethylene in the outer layer has a density of 0.930 to 0.940 g/cm3 and/or a melt index (I2) of 2.5 to 4 g/10 minutes. In some embodiments, the first polyethylene is present in the outer layer in an amount up to 50 weight percent. In some embodiments, the first polyethylene is present in the outer layer in an amount up to 20 weight percent. In some embodiments, the first polyethylene in the outer layer has a density of 0.60 to 0.970 g/cm3 and a melt index (I2) of 6 to 10 g/10 minutes.
In some embodiments, the first polymeric material of the core of the polymer particle is elastomeric and the second polymeric material of the shell of the polymer particle is a
thermoplastic. The shell, in some embodiments, comprises an acrylic polymer. In some embodiments, the polymer particles have an average size of 1 to 10 microns.
The outer layer, in some embodiments, further comprises a compatibilizer. The compatibilizer when present, in some embodiments, is a polyolefin copolymer with acrylic acid, a polyolefin copolymer with an acrylate, a polyolefin copolymer with a maleic anhydride ester, or a polyolefin copolymer grafted with one or more anhydride group, acrylate group or carboxylic acid group. In some embodiments, the compatibilizer is maleic anhydride grafted low density polyethylene or a maleic anhydride grafted high density polyethylene. In some embodiments, the compatibilizer is present in the outer layer in an amount up to 10 weight percent based on the total weight of the outer layer.
In some embodiments, the first polyethylene (in the outer layer) and the second polyethylene (in the second layer) are each high density polyethylene.
In some embodiments, the multilayer film has two matte surfaces, wherein the multilayer film has a second outer layer, wherein the second layer is between the outer layer and the second outer layer, and wherein the second outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°. In some such embodiments, the second outer layer comprises (i) 30 to 99.5 weight percent of a low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the second outer layer.
The present invention also provides articles, such as labels and packages, formed from any of the inventive multilayer films disclosed herein.
Outer Layer
The outer layer in a multilayer film advantageously provides a matte surface. As used herein, the term “matte surface” refers to a surface with a dull appearance, as opposed to a glossy appearance. A matte surface has one or both of (1) a gloss of less than 50%, and (2) a haze of greater than 45%. In some embodiments, the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°. In some embodiments, the outer layer has
a gloss of less than 45% as measured by ASTM D2457 at an angle of 45°. In some embodiments, the outer layer has a haze of greater than 45% as measured by ASTM D1003. In some embodiments, the outer layer has a haze of greater than 50% as measured by ASTM D1003. In some embodiments, the outer layer has a haze of greater than 55% as measured by ASTM DI 003.
To provide the matte surface, the outer layer comprises (i) 30 to 99.5 weight percent of a first low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, and (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, each based on the total weight of the outer layer. In some embodiments, the outer layer further comprises up to 50 weight percent of a first polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, based on the total weight of the outer layer. In some embodiments, the outer layer further comprises a compatibilizer.
The outer layer includes a first low density polyethylene having a density of 0.919 to 0.940 g/cm3. All individual values and subranges of 0.919 to 0.940 g/cm3 are included herein and disclosed herein; for example, the density of the low density polyethylene can be from a lower limit of 0.919, 0.920, 0.922, 0.925, 0.927, 0.929, or 0.930 g/ cm3 to an upper limit of 0.925, 0.930, 0.935, or 0.940 g/cm3. In some embodiments, the low density polyethylene has a density of 0.930 to 0.940 g/cm3.
In some embodiments, the low density polyethylene has a melt index (I2) 0.3 to 5 g/10 minutes. All individual values and subranges from 0.3 to 5 g/10 minutes are included herein and disclosed herein. For example, the low density polyethylene can have an I2 from a lower limit of 0.3, 0.5, 0.7, 0.9, 1.0, 1.2, 1.5, 1.8, 2.0, 2.3, 2.5, 2.7, 3.0, 3.3, or 3.5 g/10 minutes to an upper limit of 2.0, 2.5, 2.8, 3.0, 3.2, 3.5, 3.7, 4.0, 4.2, 4.5, 4.8, or 5 g/10 minutes. For example, the low density polyethylene can have an I2 of 2.5 to 4.0 g/10 minutes.
The outer layer comprises from 30 to 99.5 wt% of the low density polyethylene, based on the total weight of the outer layer. All individual values and subranges from 30 to 99.5 percent by weight (wt%) are included herein and disclosed herein; for example the amount of the low density polyethylene can be from a lower limit of 30, 35, 40, 45, 50, 55, 60, 65, 70, 76, 80, 85, or 90 wt% to an upper limit of 50, 55, 60, 65, 70, 75, 80, 85, 90, 92, 94, 96, 98,
99, or 99.5 wt%. For example, the amount of the low density polyethylene can be from 50 to 95 wt%, or in the alternative, from 70 to 95 wt%, or in the alternative, from 70 to 90 wt%, or in the alternative from 80 to 90 wt%.
Examples of low density polyethylenes that can be used in the outer layer in some embodiments include DOW™ low density polyethylenes (LDPE) commercially available from The Dow Chemical Company, such as DOW™ LDPE 525E, DOW™ LDPE 410E, DOW™ LDPE 421E, DOW™ LDPE 545E, DOW™ LDPE 555E, and DOW™ LDPE 515E.
In addition to the LDPE, the outer layer also comprises 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index.
The core/shell polymeric particles are present in amounts of at least 0.1, at least 0.5, or at least 1 weight percent based on total weight of the outer layer. The core/shell polymeric particles are present in amounts of no more than 20, no more than 15, no more than 10, no more than 7, or no more than 5 weight percent based on total weight of the outer layer. The particles can have an average particle size of at least 0.5 or at least 1 micron and no more than 15, no more than 12, or no more than 10 microns. Particle size can be determined by using conventional methods, e.g. use of a particle sizer such as Model BL90 from Brookhaven Instrument. Particle size can be measured in powder state. Particle size can show the size of agglomerated core shell particles. Core-shell particles may be purchased with a nominal particle size as specified by the vendor. The core/shell particles can be formed from acrylic monomers such as butyl acrylate, 2-ethylhexyl acrylate and lauryl methacrylate.
The core/shell polymeric particles can be characterized in that polymer in the core has a different refractive index from the refractive index of the polymer in the shell. For example, the refractive index of the polymer in the core can differ from the refractive index of the polymer in the shell by at least 0.02 or at least 0.03. Refractive index can be measured using a refractometer and following ASTM D542. The core shell material can be pressed into a thin film by hot press to facilitate this measurement.
The core/shell particles can have an elastomeric core with a thermoplastic shell. For example, the particle can have a rubber particle core formed by a polymer comprising an elastomeric or rubbery polymer as a main ingredient, optionally an intermediate layer formed with a monomer having two or more double bonds and coated on the core layer, and a shell
layer formed by a polymer graft polymerized on the core or on an intermediate layer. The shell layer partially or entirely covers the surface of the rubber particle core by graft polymerizing a monomer to the core. At least 30%, at least 40%, at least 50% or at least 60% up to 95, up to 90 up to 85 or up to 80% of the weight of the particle can be the core.
Generally, the polymer constituting the rubber particle core can have a glass transition temperature (Tg) of 0° C or lower or -30° C or lower. Tg can be determined by DSC measurement or can be calculated for copolymers using the Fox equation [Bulletin of the American Physical Society 1, 3 Page 123 (1956)] as follows: 1 Tg = wi x Tg(i> + W2 Tg(2>. For a copolymer, wi and W2 refer to the weight fraction of the two comonomers, and Tg<i) and Tg(2) refer to the glass transition temperatures of the two corresponding homopolymers in Kelvin. For polymers containing three or more monomers, additional terms are added (wn and Tg(n)). The Tg of a polymer phase can also be calculated by using the appropriate values for the glass transition temperatures of homopolymers, which may be found, for example, in “Polymer Handbook”, edited by J. Brandrup and E. H. Immergut, Interscience Publishers.
The polymer constituting the rubber particle core can be made from an elastomeric material comprising from 50 weight percent to 100 weight percent of at least one member selected from diene monomers (conjugated diene monomers) and (meth)acrylic acid ester monomers and 0 to 50 weight percent of other copolymerizable vinyl monomers, polysiloxane type elastomers or combinations thereof wherein the weight percents are based on total weight of the elastomeric material. The term “(meth)acryl” is defined as acryl and/or methacryl.
The diene monomer (conjugated diene monomer) used in making the elastomeric material can include but is not limited to, for example, butadiene, isoprene and chloroprene. Butadiene can be used in some embodiments. Further, the (meth)acrylic ester monomer can include, for example, butyl acrylate, 2-ethylhexyl acrylate, and lauryl methacrylate, and can be used alone or in combination.
Further, the above-mentioned elastomeric materials of a diene monomer or (meth) acrylate ester monomer can also be a copolymer of a vinyl monomer copolymerizable therewith. The vinyl monomer copolymerizable with the diene monomer or (meth)acrylic ester monomers can include, for example, aromatic vinyl monomers and vinyl cyanate monomers. Examples of aromatic vinyl monomers that can be used include but are not limited to styrene, alpha-methylstyrene, and vinyl naphthalene, while examples of vinyl
cyanate monomers that can be used include but are not limited to (meth) acrylonitrile and substituted acrylonitrile. The aromatic vinyl monomers and vinyl cyanate monomers can be used alone or in combination.
The amount of the diene monomer or (meth)acrylic ester monomer used can be in the range of from 50 weight percent to 100 weight percent or from 60 weight percent to 100 weight percent based on the entire weight of the elastomeric material. If the amount of the diene monomer or (meth)acrylic ester monomer to be used for the entire rubber elastomer is less than 50 weight percent, the ability of the polymer particles to toughen a polymer network, such as a cured epoxy matrix, is decreased. The amount of the monomer copolymerizable therewith can be 50 weight percent or less or 40 weight percent or less based on the entire weight of the elastomeric material.
Further, as an ingredient constituting the elastomeric material, a polyfunctional monomer can also be included for controlling the degree of crosslinking. The polyfunctional monomer can include, for example, divinylbenzene, butanediol di(meth)acrylate, triallyl (iso)cyanurate, allyl(meth) acrylic, diallyl itaconate, and diallyl phthalate. The polyfunctional monomer can be used in an amount in the range of from 0 weight percent to 10 weight percent, from 0 weight percent to 3 weight percent, or from 0 weight percent to 0.3 weight percent, based on the entire weight of the elastomeric material. In the case where the amount of the polyfunctional monomer exceeds 10 weight percent, the ability of the polymer particles to toughen a polymer network can be decreased.
Optionally, a chain transfer agent can be used for controlling the molecular weight or the crosslinking density of the polymer constituting the elastomeric material. The chain transfer agent can include, for example, an alkylmercaptan containing from 5 to 20 carbon atoms. The amount of the chain transfer agent in the recipe can be in the range of from 0 weight percent to 5 weight percent, or from 0 weight percent to 3 weight percent based on the entire weight of the elastomeric material. In the case where the amount exceeds 5 weight percent, the amount of the non-crosslinked portion in the rubber particle core increases, which can result in undesired effects on the heat resistance, rigidity, etc. of the composition when it is incorporated into an epoxy resin composition.
A polysiloxane type elastomer can be used in place of the elastomeric material described above as the rubber particle core or in combination therewith. In the case where the polysiloxane type elastomer is used as the rubber particle core, a polysiloxane type elastomer
constituted of dialkyl or diaryl substituted silyloxy unit, for example, dimethyl silyloxy, methylphenyl silyloxy, and diphenyl silyloxy can be used. When using such a polysiloxane type elastomer, a crosslinked structure can be introduced by using a polyfunctional alkoxy silane compound or with radial polymerization of silane compound having a vinylic reactive group.
The polymer particles can be configured to have an intermediate layer between an elastic core layer and a shell layer. The intermediate layer is formed by using a monomer (hereinafter, sometimes referred to as a “monomer for intermediate layer formation”) having two or more polymerizable (radical polymerizable) double bonds in a single molecule. Through one of the double bonds, the monomer for intermediate layer formation is graft- polymerized with a polymer forming the elastic core layer to substantially chemically bond the intermediate layer and the shell layer and, at the same time, through the remaining double bond(s), can crosslink the surface of the elastic core layer or can bond to the shell layer. This can improve the grafting efficiency of the shell layer, since many double bonds are arranged in the elastic core layer. The intermediate layer is present in an amount of from 0 or from 0.2 weight percent to 7 weight percent of the polymer particles. The monomer having two or more double bonds and can be selected from the group consisting of (meth) acrylate type polyfunctional monomers, isocyanuric acid derivatives, aromatic vinyl type polyfunctional monomers, and aromatic polycarboxylic acid esters. Radical polymerizable double bonds are more efficient to form a crosslinked layer that covers surface of the elastic core layer. The mass of the monomers forming the intermediate layer equals the mass of the intermediate layer, assuming all monomers added to the formulation participated in the reaction to form the intermediate layer.
The shell layer can be graft polymerized with the polymer constituting the rubber particle core, substantially forming a chemical bond with the polymer constituting the core directly or via the intermediate layer. At least 70 weight percent, at least 80 weight percent, or at least 90 weight percent of the polymer constituting the shell layer can be bonded with the core.
The polymer constituting the shell layer can be a polymer or copolymer obtained by polymerizing or copolymerizing one or more ingredients selected from the group consisting of (meth)acrylic esters, aromatic vinyl compounds, vinyl cyanate compounds, unsaturated acid derivatives, (meth)acrylamide derivatives and maleimide derivatives.
Examples of the (meth)acrylic esters that can be used include, but are not limited to alky l(meth) acrylate esters such as methyl(meth)acrylate, ethyl(meth)acrylate, butyl(meth)acrylate, and 2-ethylhexyl(meth)acrylate. Examples of the aromatic vinyl compounds include, but are not limited to styrene, a-methylstyrene, alkyl-substituted styrene, and halogen-substituted styrenes such as bromo styrene or chloro styrene.
Examples of vinyl cyanate compounds include, but are not limited to (meth) acrylonitrile and substituted acrylonitrile. Examples of the monomers containing the reactive functional group include, but are not limited to 2-hydroxylethyl (meth)acrylate, 2- aminoethyl(meth)acrylate, glycidyl(meth)acrylate, and (meth) acrylate esters having a reactive side chain. Examples of the vinyl ether containing a reactive group include but are not limited to glycidyl vinyl ether and allyl vinyl ether. Examples of the unsaturated carboxylic acid derivatives include but are not limited to (meth)acrylic acid, itaconic acid, chrotonic acid and maleic acid anhydride. Examples of (meth)acrylamide derivatives include, but are not limited to (meth)acrylamide (including N-substituted products).
Examples maleimide derivatives include but are not limited to maleic acid imide (including N-substitution products).
The shell polymer can comprise at least 5, at least 10, at least 15 or at least 20% up to 70, up to 60, or up to 50% by weight based on total weight of the particle.
The weight ratio of the core layer to the shell layer of a preferred rubber particle can be in the range of from at least 30:70, at least 40:60, or at least 50:50 up to 95:5, up to 90:10, up to 85:15, or up to 80:20.
The shell can have a Tg of at least 50, at least 70, or at least 100 °C.
The core/shell polymer particles can be produced by a variety of well-known methods, for example, emulsion polymerization, suspension polymerization, or microsuspension polymerization. Among them, a production process by the emulsion polymerization is suitable from the view point that it is easy to design composition of the core/shell polymer particles, and it is easy to produce the particles at an industrial scale and maintain quality of the rubbery polymer particles suitable to the process of this invention. As the emulsifying or dispersing agent in an aqueous medium, it is preferred to use those that maintain emulsifying or dispersion stability even in the case where pH of the aqueous latex is neutral. Specifically, they include, for example, nonionic emulsifier or dispersant such as alkali metal salts or ammonium salts of various acids, for example, alkyl or aryl sulfonic
acids typically represented by dioctyl sulfosuccinic acid or dodecylbenzene sulfonic acid, alkyl or aryl sulfonic acid typically represented by dodecyl sulfonic acid, alkyl or aryl ether sulfonic acid, alkyl or aryl substituted phosphoric acid, alkyl or aryl ether substituted phosphoric acid, or N-alkyl or aryl sarcosinic acid typically represented by dodecyl sarcosinic acid, alkyl or aryl carboxylic acid typically represented by oleic acid or stearic acid, alkyl or aryl ether carboxylic acids, and alkyl or aryl substituted polyethylene glycol, and dispersant such as polyvinyl alcohol, alkyl substituted cellulose, polyvinyl pyrrolidone or polyacrylic acid derivative. They may be used alone or in combination of two or more.
The particle can have an alkylacrylate copolymer core surrounded by a methyl methacrylate copolymer shell. The particle can have a core with a Tg of less than 0 °C and the shell has a Tg of at least 100 °C. Commercially available particles that are suitable include PARALOID™ EXL 5136 from The Dow Chemical Company.
The outer layer can comprise more than one (e.g., 2 or 3) types of polymeric particle as described above.
In some embodiments, the outer layer may further comprise a first polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (D) of 0.8 to 10 g/10 minutes. The first polyethylene is different from the first low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes discussed above.
The first polyethylene that may be used in the outer layer has a density of 0.925 to 0.970 g/cm3. All individual values and subranges of 0.925 to 0.970 g/cm3 are included herein and disclosed herein; for example, the density of the first polyethylene can be from a lower limit of 0.925, 0.930, 0.935, 0.940, 0.945, 0.950, 0.955, or 0.960 g/ cm3 to an upper limit of 0.945, 0.950, 0.955, 0.960, 0.965, or 0.970 g/cm3. In some embodiments, the first polyethylene has a density of 0.960 to 0.970 g/cm3.
In some embodiments, the first polyethylene has a melt index (I2) 0.8 to 10 g/10 minutes. All individual values and subranges from 0.8 to 10 g/10 minutes are included herein and disclosed herein. For example, the first polyethylene can have an I2 from a lower limit of 0.8, 1.0, 1.2, 1.5, 1.8, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, or 6.5 g/10 minutes to an upper limit of 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, or 10 g/10 minutes. For example, the first polyethylene can have an I2 of 6 to 10 g/10 minutes.
The first polyethylene can be an optional component in the outer in some embodiments. In embodiments where the outer layer includes the first polyethylene, the outer layer comprises up to 50 wt% of the first polyethylene, based on the total weight of the outer layer. All individual values and subranges up to 50 percent by weight (wt%) are included herein and disclosed herein; for example the amount of the first polyethylene can be from a lower limit of 1, 3, 5, 10, 15, 20, 25, 30, 35 or 40 wt% to an upper limit of 5, 10, 15, 20, 25, 30, 35, 40, 45, or 50. For example, the amount of the first polyethylene can be up to 20 wt%, or in the alternative, from 1 to 20 wt%, or in the alternative, from 5 to 20 wt%.
Examples of polyethylenes that can be used as the first polyethylene in the outer layer include, for example, low density polyethylene, linear low density polyethylene, medium density polyethylene, enhanced polyethylene, and high density polyethylene. In some embodiments, the first polyethylene is a high density polyethylene. Examples of commercially available polyethylenes that can be used as the first polyethylene include DOWLEX™ 2006G high density polyethylene, ELITE™ 5960G1 enhanced polyethylene, DOWLEX™ 2750ST high density polyethylene, ELITE™ 5940ST enhanced polyethylene, DOWLEX™ 2740G polyethylene, DOWLEX™ 2062GC polyethylene, and ELITE™ AT 6900 enhanced polyethylene, each of which are available from The Dow Chemical Company.
In some embodiments, the outer layer of the inventive multilayer film further comprises a compatibilizer. The compatibilizer can advantageously provide a smooth dispersion of the polymer particles within the base resin (e.g., the first low density polyethylene and any additional polyethylene). The compatibilizer is a polymer characterized in that it has similar chemical structure to the base polymer and has pendant and/or end groups that have an affinity to the core/shell polymer particle. Thus, where the base polymer is a polyolefin, the compatibilizer can be the same class of polyolefin (e.g. if the base polymer is a polyethylene the compatibilizer advantageously can be a polyethylene functionalized with a group having affinity to the shell material). In various embodiments, the compatibilizer can be a polyolefin/acrylate copolymer (e.g., polyethylene/acrylate copolymer such as ELVALOY AC™ from The Dow Chemical Company) or a polyolefin/acrylic acid copolymer (e.g., polyethylene/acrylic acid copolymer such as NUCREL™ from The Dow Chemical Company), or a polyolefin/carboxylic acid copolymer, or a polyolefin/maleic anhydride ester copolymer. In some embodiments, a polyolefin based compatibilizer can be grafted with one or more anhydride groups or acrylate groups or acrylic
acid groups. For example, if the base polymer comprises LDPE as its sole or major component, the compatibilizer can be a polyethylene such as an LDPE or HDPE grafted with an anhydride group such as maleic anhydride. One example is FUSABOND™ E265 from The Dow Chemical Company. The amount of compatibilizer can be from 0.5 or from 1 weight percent up to 30, up to 20, up to 15, or up to 10 weight percent based on total weight of the outer layer. In some embodiments, the amount of compatibilizer is 0.5 to 10 weight percent based on the total weight of the outer layer. The amount of the compatibilizer may increase as the amount of acrylic polymer particle increases. The compatibilizer can be a mixture of polymers as described above as compatibilizers.
The outer layer of the multilayer film may contain one or more additives as is generally known in the art. Such additives include antioxidants, such as IRGANOX 1010 and IRGAFOS 168 (commercially available from BASF), ultraviolet light absorbers, antistatic agents, pigments, dyes, nucleating agents, fillers, slip agents, fire retardants, plasticizers, processing aids, lubricants, stabilizers, smoke inhibitors, viscosity control agents, surface modification agents, and anti-blocking agents. Second Layer
Multilayer films according to embodiments of the present invention further comprise a second layer in adhering contact with the outer surface. In some embodiments, the second layer comprises (i) 1 to 80 weight percent of a second low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, and (ii) 20 to 99 weight percent of a second polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the outer layer. In some embodiments, the second low density polyethylene used in the second layer is the same as the first low density polyethylene used in the outer layer (i.e., the same density, melt index (I2), and polymeric architecture). In some embodiments, the second polyethylene used in the second layer is the same as the first polyethylene used in the outer layer (i.e., the same density, melt index (I2), and polymeric architecture). In some embodiments, the second low density polyethylene used in the second layer is the same as the first low density polyethylene used in the outer layer, and the second polyethylene used in the second layer is the same as the first polyethylene used in the outer layer.
Regarding the second low density polyethylene used in the second layer, the low density polyethylene having a density of 0.919 to 0.940 g/cm3. All individual values and
subranges of 0.919 to 0.940 g/cm3 are included herein and disclosed herein; for example, the density of the second low density polyethylene can be from a lower limit of 0.919, 0.920, 0.922, 0.925, 0.927, 0.929, or 0.930 g/ cm3 to an upper limit of 0.925, 0.930, 0.935, or 0.940 g/cm3. In some embodiments, the second low density polyethylene has a density of 0.930 to 0.940 g/cm3.
In some embodiments, the second low density polyethylene has a melt index (I2) 0.3 to 5 g/10 minutes. All individual values and subranges from 0.3 to 5 g/10 minutes are included herein and disclosed herein. For example, the second low density polyethylene can have an I2 from a lower limit of 0.3, 0.5, 0.7, 0.9, 1.0, 1.2, 1.5, 1.8, 2.0, 2.3, 2.5, 2.7, 3.0, 3.3, or 3.5 g/10 minutes to an upper limit of 2.0, 2.5, 2.8, 3.0, 3.2, 3.5, 3.7, 4.0, 4.2, 4.5, 4.8, or 5 g/10 minutes. For example, the second low density polyethylene can have an I2 of 2.5 to 4.0 g/10 minutes.
The second layer comprises from 1 to 100 wt% of the second low density polyethylene, based on the total weight of the second layer. All individual values and subranges from 1 to 80 percent by weight (wt%) are included herein and disclosed herein; for example the amount of the second low density polyethylene can be from a lower limit of 1, 3, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, or 60 wt% to an upper limit of 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, or 80 wt%. For example, the amount of the second low density polyethylene can be from 50 to 100 wt%, or in the alternative, from 60 to 100 wt%, or in the alternative, from 70 to 100 wt%.
Examples of low density polyethylenes that can be used in the second layer in some embodiments include DOW™ low density polyethylenes (LDPE) commercially available from The Dow Chemical Company, such as DOW™ LDPE 525E, DOW™ LDPE 410E, DOW™ LDPE 421E, DOW™ LDPE 545E, DOW™ LDPE 555E, and DOW™ LDPE 515E.
In addition to the LDPE, the second layer also comprises a second polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes. The second polyethylene is different from the second low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes discussed above. As noted above, the second polyethylene in the second layer can be the same as the first polyethylene used in the outer layer. In some embodiments, both the first polyethylene used in the outer layer and the second polyethylene used in the second layer can be high density polyethylenes.
The second polyethylene that may be used in the outer layer has a density of 0.925 to 0.970 g/cm3. All individual values and subranges of 0.925 to 0.970 g/cm3 are included herein and disclosed herein; for example, the density of the second polyethylene can be from a lower limit of 0.925, 0.930, 0.935, 0.940, 0.945, 0.950, 0.955, or 0.960 g/ cm3 to an upper limit of 0.945, 0.950, 0.955, 0.960, 0.965, or 0.970 g/cm3. In some embodiments, the second polyethylene has a density of 0.960 to 0.970 g/cm3.
In some embodiments, the second polyethylene has a melt index (I2) 0.8 to 10 g/10 minutes. All individual values and subranges from 0.8 to 10 g/10 minutes are included herein and disclosed herein. For example, the second polyethylene can have an I2 from a lower limit of 0.8, 1.0, 1.2, 1.5, 1.8, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, or 6.5 g/10 minutes to an upper limit of 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, or 10 g/10 minutes. For example, the second polyethylene can have an I2 of 6 to 10 g/10 minutes.
The second layer comprises from 20 to 99 wt% of the second polyethylene, based on the total weight of the second layer. All individual values and subranges from 20 to 99 percent by weight (wt%) are included herein and disclosed herein; for example the amount of the second polyethylene can be from a lower limit of 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 76, or 80 wt% to an upper limit of 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 99 wt%. For example, the amount of the second polyethylene can be from 1 to 50 wt%, or in the alternative, from 1 to 40 wt%, or in the alternative, from 1 to 30 wt%.
Examples of polyethylenes that can be used as the second polyethylene in the second layer include, for example, low density polyethylene, linear low density polyethylene, medium density polyethylene, enhanced polyethylene, and high density polyethylene. In some embodiments, the second polyethylene is a high density polyethylene. Examples of commercially available polyethylenes that can be used as the second polyethylene include DOWLEX™ 2006G high density polyethylene, ELITE™ 5960G1 enhanced polyethylene, DOWLEX™ 2750ST high density polyethylene, ELITE™ 5940ST enhanced polyethylene, DOWLEX™ 2740G polyethylene, DOWLEX™ 2062GC polyethylene, and ELITE™ AT 6900 enhanced polyethylene, each of which are available from The Dow Chemical Company.
The second layer of the multilayer film may contain one or more additives as is generally known in the art. Such additives include antioxidants, such as IRGANOX 1010 and IRGAFOS 168 (commercially available from BASF), ultraviolet light absorbers, antistatic agents, pigments, dyes, nucleating agents, fillers, slip agents, fire retardants,
plasticizers, processing aids, lubricants, stabilizers, smoke inhibitors, viscosity control agents, surface modification agents, and anti-blocking agents.
Other Layers
Multilayer films of the present invention can comprise a variety of other layers in addition to the outer layer and the second layer. Such layers would be in adhering contact with the second layer or another intervening layer. The number of layers in the multilayer film can depend on a number of factors including, for example, the desired properties of the film, the end use application, the desired thickness of the film, and others. For example, the other layers when the multilayer film is to be used in package may be different from the other layers used when the multilayer film is to be used as a label. Examples of different layers that can be used in various embodiments are discussed further herein. Multilayer films of the present invention comprise up to 13 layers in some embodiments. In various embodiments, the multilayer film comprises 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13 layers.
In some embodiments, a multilayer film of the present invention comprises a second outer layer which is a sealant layer. The sealant layer can be used to form an article or package by using the sealant layer to adhere the film to another film, to a laminate, or to itself. In some embodiments, the sealant layer can comprise any resins known to those having ordinary skill in the art to be useful as a sealant layer. Examples of polymers that can be used to form a sealant layer in some embodiments of the present invention include, without limitation, LDPE (e.g., DOW™ LDPE and AGILITY™ LDPE commercially available from The Dow Chemical Company), LLDPE (e.g., DOWLEX™ LLDPE resins commercially available from The Dow Chemical Company), polyolefin plastomers or elastomers (e.g., AFFINITY™ plastomers and elastomers commercially available from The Dow Chemical Company), ethylene vinyl acetate copolymers (e.g., ELVAX™ ethylene vinyl acetate copolymers commercially available from The Dow Chemical Company) and ionomers of ethylene acid copolymers (e.g., SURLYN™ ionomers commercially available from The Dow Chemical Company).
In some embodiments, the multilayer film comprises a second outer layer that provides a second matte surface. In some embodiments, the second outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°. In some such embodiments, the composition of the second outer layer is the same as the composition of the first outer layer. In some such embodiments, the second outer layer comprises (i) 30 to 99.5 weight
percent of a low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/ 10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the second outer layer.
In some embodiments, the multilayer film is a five layer structure wherein a first outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45° to provide the matte surface. A core or innermost layer has the composition of the second layer as described above. A second outer layer, in some embodiments, can provide a second matte surface (a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°) or can be a sealant layer as described above. Two intermediate or sub-skin layers are present with one intermediate layer between the first outer layer and the core layer, and a second intermediate layer between the second outer layer and the core layer. In some embodiments, the intermediate layers can be formed from high density polyethylene or a blend of high density polyethylene and linear low density polyethylene (with HDPE being present in the larger amount).
In some embodiments, depending on the desired use or requirements of the multilayer film, the film can comprise other layers such as barrier layers. For example, for some uses, it may be desirable for the film to provide a barrier to moisture, light, aroma/odor, and/or oxygen transmission. Such barrier layers can comprise, for example, polyamide, ethylene vinyl alcohol copolymer, and other polymers used in barrier layers as known to those of skill in the art. In such embodiments, an inner layer of the multilayer film comprises ethylene vinyl alcohol copolymer or polyamide. In some such embodiments, the multilayer film comprises 30 weight percent or less ethylene vinyl alcohol copolymer and polyamide based on the total weight of the multilayer film. In some embodiments, the multilayer film comprises 20 weight percent or less ethylene vinyl alcohol copolymer and polyamide based on the total weight of the multilayer film. In some embodiments, the multilayer film comprises 10 weight percent or less ethylene vinyl alcohol copolymer and polyamide based on the total weight of the multilayer film. In some embodiments, the multilayer film
comprises less than 5% by weight ethylene vinyl alcohol copolymer and polyamide based on the total weight of the multilayer film.
In embodiments comprising an inner layer having ethylene vinyl alcohol copolymer or polyamide, one or more tie layers may be included in the film to adhere the barrier layer(s) to the polyethylene-based layer(s) as known to those of skill in the art based on the teachings herein. In general, a wide variety of tie layer compositions can be used to form a tie layer as known to those of skill in the art based on the teachings herein.
In some embodiments, barrier properties may not be as important for the multilayer film. In some such embodiments, the multilayer film may comprise less than 0.5 weight percent ethylene vinyl alcohol copolymer and polyamide based on the total weight of the film. In some embodiments, the multilayer film comprises less than 0.1 weight percent ethylene vinyl alcohol copolymer and polyamide based on the total weight of the film. In some embodiments, the multilayer film is free of ethylene vinyl alcohol copolymer and polyamide.
In some embodiments, a multilayer film of the present invention has a total thickness of at least 30 microns. In some embodiments, the multilayer film has a thickness of up to 90 microns. In some embodiments, the multilayer film has a thickness from 30 microns to 90 microns.
Multilayer films of the present invention can exhibit one or more desirable properties. As discussed elsewhere, the multilayer films of the present invention has a matte surface. The outer layer of the multilayer film provides a matte surface in that the outer layer has one or both of (1) a gloss of less than 50%, and (2) a haze of greater than 45%. In some embodiments, the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°. In some embodiments, the outer layer has a gloss of less than 45% as measured by ASTM D2457 at an angle of 45°. In some embodiments, the outer layer has a haze of greater than 45% as measured by ASTM DI 003. In some embodiments, the outer layer has a haze of greater than 50% as measured by ASTM D1003. In some embodiments, the outer layer has a haze of greater than 55% as measured by ASTM D1003. In some embodiments, the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45° and haze of greater than 45% as measured by ASTM DI 003. In some embodiments, the outer layer has a gloss of less than 45% as measured by ASTM D2457 at an angle of 45° and haze of greater than 50% as measured by ASTM D1003. In some
embodiments, the outer layer has a gloss of less than 45% as measured by ASTM D2457 at an angle of 45° and haze of greater than 55% as measured by ASTM D1003.
Multilayer films can be coextruded as blown films or cast films using techniques known to those of skill in the art based on the teachings herein. In particular, based on the compositions of the different film layers disclosed herein, blown film manufacturing lines and cast film manufacturing lines can be configured to coextrude multilayer films of the present invention in a single extrusion step using techniques known to those of skill in the art based on the teachings herein.
Labels
Embodiments of the present invention also comprise labels formed from or incorporating multilayer films of the present invention. Such labels can be made from the inventive multilayer films using techniques known to those having ordinary skill in the art based on the teachings herein.
Packages
Embodiments of the present invention also comprise packages formed from or incorporating multilayer films of the present invention. Such packages can be made from the inventive multilayer films using techniques known to those having ordinary skill in the art based on the teachings herein.
Examples of such packages can include flexible packages, pouches, stand-up pouches, and pre-made packages or pouches. In some embodiments, multilayer films of the present invention can be used for food packages. Examples of food that can be included in such packages include meats, cheeses, cereal, nuts, juices, sauces, and others. Such packages can be formed using techniques known to those of skill in the art based on the teachings herein and based on the particular use for the package (e.g., type of food, amount of food, etc.).
TEST METHODS
Unless otherwise indicated herein, the following analytical methods are used in describing aspects of the present invention:
Melt index
Melt indices L (or 12) and I10 (or 110) were measured in accordance to ASTM D-1238 (method B) at 190°C and at 2.16 kg and 10 kg load, respectively. Their values are reported in g/10 min.
Density
Samples for density measurement were prepared according to ASTM D4703. Measurements were made, according to ASTM D792, Method B, within one hour of sample pressing.
Haze
Haze was measured according to ASTM D 1003. A Hazegard Plus (BYK-Gardner USA; Columbia, MD) was used for testing. For each test, 5 samples were examined, and an average was reported. An area having a diameter of six centimeters was measured on each film sample.
Gloss
Gloss at an angle of 45° was measured according to ASTM D2457 on a BYK- Gardner (Columbia, MD) micro-gloss 45 degree gloss meter (Columbia, MD). MD and CD Elmendorf Tear Strength
Elmendorf tear strength in the machine and cross directions are measured in accordance with ASTM D1922. The force in grams required to propagate tearing across a film or sheeting specimen is measured using a precisely calibrated pendulum device. Acting by gravity, the pendulum swings through an arc, tearing the specimen from a precut slit. The specimen is held on one side by the pendulum and on the other side by a stationary member. The loss in energy by the pendulum is indicated by a pointer or by an electronic scale. The scale indication is a function of the force required to tear the specimen. The sample used is the ‘constant radius geometry’ as specified in D1922. Testing would be typically carried out on samples that have been cut from both the MD and CD directions. Prior to testing, the sample thickness is measured at the sample center. A total of 10 specimens per direction are tested, and the average tear strength is reported. Samples that tear at an angle greater than 60° from the vertical are described as ‘oblique’ tears - such tears should be noted, though the strength values are included in the average strength calculation. Some embodiments of the invention will now be described in detail in the following Examples.
Examples
The following materials are used to make a variety of inventive and comparative films as discussed further below:
• DOW™ LDPE 525E (hereinafter “LDPE”): low density polyethylene having a density of 0.9315 g/cm3 and a melt index (I2) of 3.2 g/10 minutes.
• DOWLEX™ 2006 (hereinafter “HDPE”): high density polyethylene having a density of 0.963 g/cm3 and a melt index (I2) of 8 g/10 minutes. • PARALOID™ EXL-5136 (hereinafter “Polymer Particles”): polymer particles having a core and a shell structure. The polymeric material used in the core is elastomeric and has a glass transition temperature (Tg) of < 0 °C. The polymeric material used in the shell is thermoplastic and has a glass transition temperature (Tg) of > 100 °C. The polymeric material in the core has a refractive index that is different from the refractive index of the polymeric material in the shell. The average particle size of the Polymer Particles is between 1 and 10 microns.
• FUSABOND™ E265 (hereinafter “Compatibilizer”): High density polyethylene grafted with maleic anhydride having a density of 0.950 g/cm3 and a melt index (I2) of 12 g/10 minutes. Each of these materials are commercially available from The Dow Chemical Company. The following films, having structures of Layer A/Layer B/Layer C, are made:
* These components are melt blended prior to being provided to the blown film line.
In the above Inventive Films that include Polymer Particles, the Polymer Particles are melt blended with the LDPE and Compatibilizer (if present) prior to being provided to the blown film line. The blends are melt blended on a Buss Kneader Compounder at 120 rpm (kneader speed), 3 amps (motor current), 5 kg/h, 60 rpm (screw speed), and a temperature profile of 110 °C/130 °C/140 °C/120 °C/125 °C.
The above Comparative and Inventive Films are coextruded on a Dr. Collin 3 -layer Coextrusion Blown Film line. The nominal film thickness is 80 microns. The line was comprised of three 25:1 L/D single screw extruders, equipped with grooved feed zones.
Screw diameters are 25 mm for the two outer layer extruders and 30 mm for the inner layer extruder (formed from Layer B). The melt temperature is 180° C-21O0 C. The die diameter is 30 mm, and the die gap is 1.8 mm. The blow-up ratio is 2.5:1. The output rate is 15 kg/hour. The gloss at 45° and the haze of the Comparative and Inventive Films are measured as described in the Test Methods section. The results are shown in Table 2:
The effect of the addition of the Polymer Particles to a film can be observed in Table 2. Adding up to 2.5 weight percent of Polymer Particles (Inventive Film 2) in one or more outer layers led to a reduction of gloss of 59% and an increase in haze of 358%. Increasing the concentration of Polymer Particles in one or more outer layers up to 3.75 weight percent combined with compatibilizer up to 6.25 weight percent (Inventive Films 3-5) resulted in further improvement, with a 62% reduction in gloss and an increase in haze of up to 425%. The reduction in gloss is of particular interest for matte film applications, such as labels, because a less shiny surface is perceived as more natural. The Elmendorf tear strength of the films in the machine direction (MD) and cross direction (CD) are also measured as described in the Test Methods section above. The results are shown in Table 3:
Table 3
As shown in Table 3, the inclusion of Polymer Particles did not result in a significant impact on Elmendorf tear strength in the cross direction. While there was a negative impact on Elmendorf tear strength in the machine direction, this is only in relation to the monomaterial film (Comparative Film A).
Claims
1. A multilayer film having at least one matte surface comprising:
(a) an outer layer comprising (i) 30 to 99.5 weight percent of a first low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, (ii) 0.1 to 20 weight percent of polymer particles having a core and a shell structure wherein the core comprises a first polymeric material having a first refractive index and the shell comprises a second polymeric material having a second refractive index that is different from the first refractive index, and (iii) optionally, up to 50 weight percent of a first polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the outer layer; and
(b) a second layer in adhering contact with the outer layer comprising (i) 1 to 80 weight percent of a second low density polyethylene having a density of 0.919 g/cm3 to 0.940 g/cm3 and a melt index (I2) of 0.3 to 5 g/10 minutes, and (ii) 20 to 99 weight percent of a second polyethylene having a density of 0.925 g/cm3 to 0.970 g/cm3 and a melt index (I2) of 0.8 to 10 g/10 minutes, each based on the total weight of the second layer; wherein the outer layer has a gloss of less than 50% as measured by ASTM D2457 at an angle of 45°.
2. The multilayer film of claim 1, wherein the first polymeric material of the core of the polymer particle is elastomeric and the second polymeric material of the shell of the polymer particle is a thermoplastic.
3. The multilayer film of claim 1 or claim 2, wherein the shell comprises an acrylic polymer.
4. The multilayer film of any of the preceding claims, wherein the polymer particles have an average size of 1 to 10 microns.
5. The multilayer film of any of the preceding claims, wherein the outer layer further comprises a compatibilizer.
27
6. The multilayer film of claim 5, wherein the compatibilizer is a polyolefin copolymer with acrylic acid, a polyolefin copolymer with an acrylate, a polyolefin copolymer with a maleic anhydride ester, or a polyolefin copolymer grafted with one or more anhydride group, acrylate group or carboxylic acid group.
7. The multilayer film of claim 5, wherein the compatibilizer is maleic anhydride grafted low density polyethylene or a maleic anhydride grafted high density polyethylene.
8. The multilayer film of any of claims 5 to 7, wherein the compatibilizer is present in the outer layer in an amount up to 10 weight percent based on the total weight of the outer layer.
9. The multilayer film of any of the preceding claims, wherein the first polyethylene and the second polyethylene are each high density polyethylene.
10. A label comprising the multilayer film of any of the preceding claims.
11. A package comprising the multilayer film of any of claims 1 to 9.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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CN202180074718.3A CN116390851A (en) | 2020-11-20 | 2021-10-04 | Multilayer film having at least one matte surface |
US18/044,615 US20230356512A1 (en) | 2020-11-20 | 2021-10-04 | Multilayer films having at least one matte surface |
JP2023528287A JP2023552968A (en) | 2020-11-20 | 2021-10-04 | Multilayer film with at least one matte side |
EP21791574.3A EP4247635A1 (en) | 2020-11-20 | 2021-10-04 | Multilayer films having at least one matte surface |
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EP20383012.0A EP4000922A1 (en) | 2020-11-20 | 2020-11-20 | Multilayer films having at least one matte surface |
EP20383012.0 | 2020-11-20 |
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WO2022108670A1 true WO2022108670A1 (en) | 2022-05-27 |
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PCT/US2021/053369 WO2022108670A1 (en) | 2020-11-20 | 2021-10-04 | Multilayer films having at least one matte surface |
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US (1) | US20230356512A1 (en) |
EP (2) | EP4000922A1 (en) |
JP (1) | JP2023552968A (en) |
CN (1) | CN116390851A (en) |
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WO2017003543A1 (en) * | 2015-06-30 | 2017-01-05 | Dow Global Technologies Llc | Polyethylene films with matte surface |
WO2020000340A1 (en) * | 2018-06-29 | 2020-01-02 | Dow Global Technologies Llc | Biaxially-oriented polyethylene multilayer film with matte surface |
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-
2020
- 2020-11-20 EP EP20383012.0A patent/EP4000922A1/en active Pending
-
2021
- 2021-10-04 US US18/044,615 patent/US20230356512A1/en active Pending
- 2021-10-04 CN CN202180074718.3A patent/CN116390851A/en active Pending
- 2021-10-04 WO PCT/US2021/053369 patent/WO2022108670A1/en active Application Filing
- 2021-10-04 EP EP21791574.3A patent/EP4247635A1/en active Pending
- 2021-10-04 JP JP2023528287A patent/JP2023552968A/en active Pending
- 2021-11-18 AR ARP210103187A patent/AR124093A1/en unknown
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US4076698A (en) | 1956-03-01 | 1978-02-28 | E. I. Du Pont De Nemours And Company | Hydrocarbon interpolymer compositions |
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WO2020142230A1 (en) * | 2019-01-03 | 2020-07-09 | Dow Global Technologies Llc | Artificial turf grass with natural appearance |
Also Published As
Publication number | Publication date |
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EP4000922A1 (en) | 2022-05-25 |
US20230356512A1 (en) | 2023-11-09 |
EP4247635A1 (en) | 2023-09-27 |
CN116390851A (en) | 2023-07-04 |
JP2023552968A (en) | 2023-12-20 |
AR124093A1 (en) | 2023-02-15 |
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